Canonical Allele Identifier: CA2067686841
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997820_120997832delinsTCCCATGTGAATG , CM000674.2:g.120997820_120997832delinsTCCCATGTGAATG GRCh38
NC_000012.11:g.121435623_121435635delinsTCCCATGTGAATG , CM000674.1:g.121435623_121435635delinsTCCCATGTGAATG GRCh37
NC_000012.10:g.119920006_119920018delinsTCCCATGTGAATG NCBI36
NG_011731.2:g.24075_24087delinsTCCCATGTGAATG , LRG_522:g.24075_24087delinsTCCCATGTGAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*248+155_*248+167delinsTCCCATGTGAATG ENSP00000453965.2:n.*248+155_*248+167delinsTCCCATGTGAATG
ENST00000257555.11:c.1501+155_1501+167delinsTCCCATGTGAATG MANE Select ENSP00000257555.5:n.1501+155_1501+167delinsTCCCATGTGAATG
ENST00000257555.10:c.1501+155_1501+167delinsTCCCATGTGAATG ENSP00000257555.4:n.1501+155_1501+167delinsTCCCATGTGAATG
ENST00000400024.6:c.*27_*39delinsTCCCATGTGAATG ENSP00000476181.1:n.*27_*39delinsTCCCATGTGAATG
ENST00000402929.5:n.2522_2534delinsTCCCATGTGAATG
ENST00000535955.5:n.372_384delinsTCCCATGTGAATG
ENST00000538626.2:n.520_532delinsTCCCATGTGAATG
ENST00000538646.5:c.*632_*644delinsTCCCATGTGAATG ENSP00000443964.1:n.*632_*644delinsTCCCATGTGAATG
ENST00000540108.1:c.*941+155_*941+167delinsTCCCATGTGAATG ENSP00000445445.1:n.*941+155_*941+167delinsTCCCATGTGAATG
ENST00000541395.5:c.1501+155_1501+167delinsTCCCATGTGAATG ENSP00000443112.1:n.1501+155_1501+167delinsTCCCATGTGAATG
ENST00000541924.5:c.*670_*682delinsTCCCATGTGAATG ENSP00000440361.1:n.*670_*682delinsTCCCATGTGAATG
ENST00000543255.1:n.700_712delinsTCCCATGTGAATG
ENST00000543427.5:c.964+155_964+167delinsTCCCATGTGAATG ENSP00000439721.2:n.964+155_964+167delinsTCCCATGTGAATG
ENST00000544413.2:c.1501+155_1501+167delinsTCCCATGTGAATG ENSP00000438804.1:n.1501+155_1501+167delinsTCCCATGTGAATG
ENST00000544574.5:c.*419_*431delinsTCCCATGTGAATG ENSP00000438565.1:n.*419_*431delinsTCCCATGTGAATG
ENST00000560968.5:c.1318+155_1318+167delinsTCCCATGTGAATG
ENST00000615446.4:c.289+155_289+167delinsTCCCATGTGAATG ENSP00000483994.1:n.289+155_289+167delinsTCCCATGTGAATG
ENST00000617366.4:c.618+155_618+167delinsTCCCATGTGAATG ENSP00000481967.1:n.618+155_618+167delinsTCCCATGTGAATG
NM_000545.5:c.1501+155_1501+167delinsTCCCATGTGAATG , LRG_522t1:c.1501+155_1501+167delinsTCCCATGTGAATG NP_000536.5:n.1501+155_1501+167delinsTCCCATGTGAATG
NM_000545.6:c.1501+155_1501+167delinsTCCCATGTGAATG NP_000536.5:n.1501+155_1501+167delinsTCCCATGTGAATG
NM_001306179.1:c.1501+155_1501+167delinsTCCCATGTGAATG NP_001293108.1:n.1501+155_1501+167delinsTCCCATGTGAATG
XM_005253931.2:c.1501+155_1501+167delinsTCCCATGTGAATG XP_005253988.1:n.1501+155_1501+167delinsTCCCATGTGAATG
XM_024449168.1:c.1501+155_1501+167delinsTCCCATGTGAATG XP_024304936.1:n.1501+155_1501+167delinsTCCCATGTGAATG
NM_000545.8:c.1501+155_1501+167delinsTCCCATGTGAATG MANE Select NP_000536.6:n.1501+155_1501+167delinsTCCCATGTGAATG
NM_001306179.2:c.1501+155_1501+167delinsTCCCATGTGAATG NP_001293108.2:n.1501+155_1501+167delinsTCCCATGTGAATG