Canonical Allele Identifier: CA2067672684

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120988863C= , CM000674.2:g.120988863C=	GRCh38
NC_000012.11:g.121426666C= , CM000674.1:g.121426666C=	GRCh37
NC_000012.10:g.119911049C=	NCBI36
NG_011731.2:g.15118C= , LRG_522:g.15118C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.357C=	ENSP00000453965.2:p.Val119=
ENST00000257555.11:c.357C= MANE Select	ENSP00000257555.5:p.Val119=
ENST00000257555.10:c.357C=	ENSP00000257555.4:p.Val119=
ENST00000400024.6:c.357C=	ENSP00000476181.1:p.Val119=
ENST00000402929.5:n.492C=
ENST00000535955.5:n.43-8628C=
ENST00000538626.2:n.191-8628C=
ENST00000538646.5:c.357C=	ENSP00000443964.1:p.Val119=
ENST00000540108.1:c.327-4657C=	ENSP00000445445.1:n.327-4657C=
ENST00000541395.5:c.357C=	ENSP00000443112.1:p.Val119=
ENST00000541924.5:c.357C=	ENSP00000440361.1:p.Val119=
ENST00000543427.5:c.357C=	ENSP00000439721.2:p.Val119=
ENST00000544413.2:c.357C=	ENSP00000438804.1:p.Val119=
ENST00000544574.5:c.73-7754C=	ENSP00000438565.1:n.73-7754C=
ENST00000560968.5:c.500C=
ENST00000615446.4:c.-257-7399C=	ENSP00000483994.1:n.-257-7399C=
ENST00000617366.4:c.357C=	ENSP00000481967.1:p.Val119=
NM_000545.5:c.357C= , LRG_522t1:c.357C=	NP_000536.5:p.Val119=
NM_000545.6:c.357C=	NP_000536.5:p.Val119=
NM_001306179.1:c.357C=	NP_001293108.1:p.Val119=
XM_005253931.2:c.357C=	XP_005253988.1:p.Val119=
XM_024449168.1:c.357C=	XP_024304936.1:p.Val119=
NM_000545.8:c.357C= MANE Select	NP_000536.6:p.Val119=
NM_001306179.2:c.357C=	NP_001293108.2:p.Val119=