Canonical Allele Identifier: CA244532645
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs1050539560

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120993816_120993818del , CM000674.2:g.120993816_120993818del GRCh38
NC_000012.11:g.121431619_121431621del , CM000674.1:g.121431619_121431621del GRCh37
NC_000012.10:g.119916002_119916004del NCBI36
NG_011731.2:g.20071_20073del , LRG_522:g.20071_20073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.713+110_713+112del ENSP00000453965.2:n.713+110_713+112del
ENST00000257555.11:c.713+110_713+112del MANE Select ENSP00000257555.5:n.713+110_713+112del
ENST00000257555.10:c.713+110_713+112del ENSP00000257555.4:n.713+110_713+112del
ENST00000400024.6:c.713+110_713+112del ENSP00000476181.1:n.713+110_713+112del
ENST00000402929.5:n.848+110_848+112del
ENST00000535955.5:n.43-3675_43-3673del
ENST00000538626.2:n.191-3675_191-3673del
ENST00000538646.5:c.527-348_527-346del ENSP00000443964.1:n.527-348_527-346del
ENST00000540108.1:c.*153+110_*153+112del ENSP00000445445.1:n.*153+110_*153+112del
ENST00000541395.5:c.713+110_713+112del ENSP00000443112.1:n.713+110_713+112del
ENST00000541924.5:c.713+110_713+112del ENSP00000440361.1:n.713+110_713+112del
ENST00000543427.5:c.633+190_633+192del ENSP00000439721.2:n.633+190_633+192del
ENST00000544413.2:c.713+110_713+112del ENSP00000438804.1:n.713+110_713+112del
ENST00000544574.5:c.73-2801_73-2799del ENSP00000438565.1:n.73-2801_73-2799del
ENST00000560968.5:c.856+110_856+112del
ENST00000615446.4:c.-257-2446_-257-2444del ENSP00000483994.1:n.-257-2446_-257-2444del
ENST00000617366.4:c.586+237_586+239del ENSP00000481967.1:n.586+237_586+239del
NM_000545.5:c.713+110_713+112del , LRG_522t1:c.713+110_713+112del NP_000536.5:n.713+110_713+112del
NM_000545.6:c.713+110_713+112del NP_000536.5:n.713+110_713+112del
NM_001306179.1:c.713+110_713+112del NP_001293108.1:n.713+110_713+112del
XM_005253931.2:c.713+110_713+112del XP_005253988.1:n.713+110_713+112del
XM_024449168.1:c.713+110_713+112del XP_024304936.1:n.713+110_713+112del
NM_000545.8:c.713+110_713+112del MANE Select NP_000536.6:n.713+110_713+112del
NM_001306179.2:c.713+110_713+112del NP_001293108.2:n.713+110_713+112del