Canonical Allele Identifier: CA2067686259
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120997659C= , CM000674.2:g.120997659C= GRCh38
NC_000012.11:g.121435462C= , CM000674.1:g.121435462C= GRCh37
NC_000012.10:g.119919845C= NCBI36
NG_011731.2:g.23914C= , LRG_522:g.23914C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.*242C= ENSP00000453965.2:n.*242C=
ENST00000257555.11:c.1495C= MANE Select ENSP00000257555.5:p.Pro499=
ENST00000257555.10:c.1495C= ENSP00000257555.4:p.Pro499=
ENST00000400024.6:c.1495C= ENSP00000476181.1:p.Pro499=
ENST00000402929.5:n.2361C=
ENST00000535955.5:n.211C=
ENST00000538626.2:n.359C=
ENST00000538646.5:c.*471C= ENSP00000443964.1:n.*471C=
ENST00000540108.1:c.*935C= ENSP00000445445.1:n.*935C=
ENST00000541395.5:c.1495C= ENSP00000443112.1:p.Pro499=
ENST00000541924.5:c.*509C= ENSP00000440361.1:n.*509C=
ENST00000543255.1:n.539C=
ENST00000543427.5:c.958C= ENSP00000439721.2:p.Pro320=
ENST00000544413.2:c.1495C= ENSP00000438804.1:p.Pro499=
ENST00000544574.5:c.*258C= ENSP00000438565.1:n.*258C=
ENST00000560968.5:c.1312C=
ENST00000615446.4:c.283C= ENSP00000483994.1:p.Pro95=
ENST00000617366.4:c.612C= ENSP00000481967.1:p.Ala204=
NM_000545.5:c.1495C= , LRG_522t1:c.1495C= NP_000536.5:p.Pro499=
NM_000545.6:c.1495C= NP_000536.5:p.Pro499=
NM_001306179.1:c.1495C= NP_001293108.1:p.Pro499=
XM_005253931.2:c.1495C= XP_005253988.1:p.Pro499=
XM_024449168.1:c.1495C= XP_024304936.1:p.Pro499=
NM_000545.8:c.1495C= MANE Select NP_000536.6:p.Pro499=
NM_001306179.2:c.1495C= NP_001293108.2:p.Pro499=