Canonical Allele Identifier: CA6831731
Gene: HNF1A HGNC NCBI

Linked Data

dbSNP Id: rs760155925

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120988801_120988802insTTGAGCAGATCCCGTC , CM000674.2:g.120988801_120988802insTTGAGCAGATCCCGTC GRCh38
NC_000012.11:g.121426604_121426605insTTGAGCAGATCCCGTC , CM000674.1:g.121426604_121426605insTTGAGCAGATCCCGTC GRCh37
NC_000012.10:g.119910987_119910988insTTGAGCAGATCCCGTC NCBI36
NG_011731.2:g.15056_15057insTTGAGCAGATCCCGTC , LRG_522:g.15056_15057insTTGAGCAGATCCCGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000453965.2:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000257555.11:c.327-32_327-31insTTGAGCAGATCCCGTC MANE Select ENSP00000257555.5:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000257555.10:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000257555.4:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000400024.6:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000476181.1:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000402929.5:n.462-32_462-31insTTGAGCAGATCCCGTC
ENST00000535955.5:n.43-8690_43-8689insTTGAGCAGATCCCGTC
ENST00000538626.2:n.191-8690_191-8689insTTGAGCAGATCCCGTC
ENST00000538646.5:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000443964.1:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000540108.1:c.327-4719_327-4718insTTGAGCAGATCCCGTC ENSP00000445445.1:n.327-4719_327-4718insTTGAGCAGATCCCGTC
ENST00000541395.5:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000443112.1:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000541924.5:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000440361.1:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000543427.5:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000439721.2:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000544413.2:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000438804.1:n.327-32_327-31insTTGAGCAGATCCCGTC
ENST00000544574.5:c.73-7816_73-7815insTTGAGCAGATCCCGTC ENSP00000438565.1:n.73-7816_73-7815insTTGAGCAGATCCCGTC
ENST00000560968.5:c.470-32_470-31insTTGAGCAGATCCCGTC
ENST00000615446.4:c.-257-7461_-257-7460insTTGAGCAGATCCCGTC ENSP00000483994.1:n.-257-7461_-257-7460insTTGAGCAGATCCCGTC
ENST00000617366.4:c.327-32_327-31insTTGAGCAGATCCCGTC ENSP00000481967.1:n.327-32_327-31insTTGAGCAGATCCCGTC
NM_000545.5:c.327-32_327-31insTTGAGCAGATCCCGTC , LRG_522t1:c.327-32_327-31insTTGAGCAGATCCCGTC NP_000536.5:n.327-32_327-31insTTGAGCAGATCCCGTC
NM_000545.6:c.327-32_327-31insTTGAGCAGATCCCGTC NP_000536.5:n.327-32_327-31insTTGAGCAGATCCCGTC
NM_001306179.1:c.327-32_327-31insTTGAGCAGATCCCGTC NP_001293108.1:n.327-32_327-31insTTGAGCAGATCCCGTC
XM_005253931.2:c.327-32_327-31insTTGAGCAGATCCCGTC XP_005253988.1:n.327-32_327-31insTTGAGCAGATCCCGTC
XM_024449168.1:c.327-32_327-31insTTGAGCAGATCCCGTC XP_024304936.1:n.327-32_327-31insTTGAGCAGATCCCGTC
NM_000545.8:c.327-32_327-31insTTGAGCAGATCCCGTC MANE Select NP_000536.6:n.327-32_327-31insTTGAGCAGATCCCGTC
NM_001306179.2:c.327-32_327-31insTTGAGCAGATCCCGTC NP_001293108.2:n.327-32_327-31insTTGAGCAGATCCCGTC