Canonical Allele Identifier: CA2067682916

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996271A= , CM000674.2:g.120996271A=	GRCh38
NC_000012.11:g.121434074A= , CM000674.1:g.121434074A=	GRCh37
NC_000012.10:g.119918457A=	NCBI36
NG_011731.2:g.22526A= , LRG_522:g.22526A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000545.8:c.965A= MANE Select	NP_000536.6:p.Tyr322=
ENST00000257555.11:c.965A= MANE Select	ENSP00000257555.5:p.Tyr322=
NM_000545.5:c.965A= , LRG_522t1:c.965A=	NP_000536.5:p.Tyr322=
NM_000545.6:c.965A=	NP_000536.5:p.Tyr322=
NM_001306179.1:c.965A=	NP_001293108.1:p.Tyr322=
NM_001306179.2:c.965A=	NP_001293108.2:p.Tyr322=
ENST00000257555.10:c.965A=	ENSP00000257555.4:p.Tyr322=
ENST00000400024.6:c.965A=	ENSP00000476181.1:p.Tyr322=
ENST00000402929.5:n.1100A=
ENST00000535955.5:n.43-1220A=
ENST00000538626.2:n.191-1220A=
ENST00000538646.5:c.778A=	ENSP00000443964.1:p.Met260=
ENST00000540108.1:c.*405A=	ENSP00000445445.1:n.*405A=
ENST00000541395.5:c.965A=	ENSP00000443112.1:p.Tyr322=
ENST00000541924.5:c.723A=	ENSP00000440361.1:p.Leu241=
ENST00000543427.5:c.634-333A=	ENSP00000439721.2:n.634-333A=
ENST00000544413.2:c.965A=	ENSP00000438804.1:p.Tyr322=
ENST00000544574.5:c.73-346A=	ENSP00000438565.1:n.73-346A=
ENST00000560968.5:c.894-112A=
ENST00000560968.6:c.751-112A=	ENSP00000453965.2:n.751-112A=
ENST00000615446.4:c.-248A=	ENSP00000483994.1:n.-248A=
ENST00000617366.4:c.587-1363A=	ENSP00000481967.1:n.587-1363A=
XM_005253931.2:c.965A=	XP_005253988.1:p.Tyr322=
XM_024449168.1:c.965A=	XP_024304936.1:p.Tyr322=