Canonical Allele Identifier: CA2067672409
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120988679_120988685delinsCCTGAGT , CM000674.2:g.120988679_120988685delinsCCTGAGT GRCh38
NC_000012.11:g.121426482_121426488delinsCCTGAGT , CM000674.1:g.121426482_121426488delinsCCTGAGT GRCh37
NC_000012.10:g.119910865_119910871delinsCCTGAGT NCBI36
NG_011731.2:g.14934_14940delinsCCTGAGT , LRG_522:g.14934_14940delinsCCTGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.327-154_327-148delinsCCTGAGT ENSP00000453965.2:n.327-154_327-148delinsCCTGAGT
ENST00000257555.11:c.327-154_327-148delinsCCTGAGT MANE Select ENSP00000257555.5:n.327-154_327-148delinsCCTGAGT
ENST00000257555.10:c.327-154_327-148delinsCCTGAGT ENSP00000257555.4:n.327-154_327-148delinsCCTGAGT
ENST00000400024.6:c.327-154_327-148delinsCCTGAGT ENSP00000476181.1:n.327-154_327-148delinsCCTGAGT
ENST00000402929.5:n.462-154_462-148delinsCCTGAGT
ENST00000535955.5:n.43-8812_43-8806delinsCCTGAGT
ENST00000538626.2:n.191-8812_191-8806delinsCCTGAGT
ENST00000538646.5:c.327-154_327-148delinsCCTGAGT ENSP00000443964.1:n.327-154_327-148delinsCCTGAGT
ENST00000540108.1:c.327-4841_327-4835delinsCCTGAGT ENSP00000445445.1:n.327-4841_327-4835delinsCCTGAGT
ENST00000541395.5:c.327-154_327-148delinsCCTGAGT ENSP00000443112.1:n.327-154_327-148delinsCCTGAGT
ENST00000541924.5:c.327-154_327-148delinsCCTGAGT ENSP00000440361.1:n.327-154_327-148delinsCCTGAGT
ENST00000543427.5:c.327-154_327-148delinsCCTGAGT ENSP00000439721.2:n.327-154_327-148delinsCCTGAGT
ENST00000544413.2:c.327-154_327-148delinsCCTGAGT ENSP00000438804.1:n.327-154_327-148delinsCCTGAGT
ENST00000544574.5:c.73-7938_73-7932delinsCCTGAGT ENSP00000438565.1:n.73-7938_73-7932delinsCCTGAGT
ENST00000560968.5:c.470-154_470-148delinsCCTGAGT
ENST00000615446.4:c.-257-7583_-257-7577delinsCCTGAGT ENSP00000483994.1:n.-257-7583_-257-7577delinsCCTGAGT
ENST00000617366.4:c.327-154_327-148delinsCCTGAGT ENSP00000481967.1:n.327-154_327-148delinsCCTGAGT
NM_000545.5:c.327-154_327-148delinsCCTGAGT , LRG_522t1:c.327-154_327-148delinsCCTGAGT NP_000536.5:n.327-154_327-148delinsCCTGAGT
NM_000545.6:c.327-154_327-148delinsCCTGAGT NP_000536.5:n.327-154_327-148delinsCCTGAGT
NM_001306179.1:c.327-154_327-148delinsCCTGAGT NP_001293108.1:n.327-154_327-148delinsCCTGAGT
XM_005253931.2:c.327-154_327-148delinsCCTGAGT XP_005253988.1:n.327-154_327-148delinsCCTGAGT
XM_024449168.1:c.327-154_327-148delinsCCTGAGT XP_024304936.1:n.327-154_327-148delinsCCTGAGT
NM_000545.8:c.327-154_327-148delinsCCTGAGT MANE Select NP_000536.6:n.327-154_327-148delinsCCTGAGT
NM_001306179.2:c.327-154_327-148delinsCCTGAGT NP_001293108.2:n.327-154_327-148delinsCCTGAGT