Canonical Allele Identifier: CA2067685778

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120997546C= , CM000674.2:g.120997546C=	GRCh38
NC_000012.11:g.121435349C= , CM000674.1:g.121435349C=	GRCh37
NC_000012.10:g.119919732C=	NCBI36
NG_011731.2:g.23801C= , LRG_522:g.23801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.*129C=	ENSP00000453965.2:n.*129C=
ENST00000257555.11:c.1382C= MANE Select	ENSP00000257555.5:p.Pro461=
ENST00000257555.10:c.1382C=	ENSP00000257555.4:p.Pro461=
ENST00000400024.6:c.1382C=	ENSP00000476181.1:p.Pro461=
ENST00000402929.5:n.2248C=
ENST00000535955.5:n.98C=
ENST00000538626.2:n.246C=
ENST00000538646.5:c.*358C=	ENSP00000443964.1:n.*358C=
ENST00000540108.1:c.*822C=	ENSP00000445445.1:n.*822C=
ENST00000541395.5:c.1382C=	ENSP00000443112.1:p.Pro461=
ENST00000541924.5:c.*396C=	ENSP00000440361.1:n.*396C=
ENST00000543255.1:n.426C=
ENST00000543427.5:c.845C=	ENSP00000439721.2:p.Pro282=
ENST00000544413.2:c.1382C=	ENSP00000438804.1:p.Pro461=
ENST00000544574.5:c.*145C=	ENSP00000438565.1:n.*145C=
ENST00000560968.5:c.1199C=
ENST00000615446.4:c.170C=	ENSP00000483994.1:p.Pro57=
ENST00000617366.4:c.587-88C=	ENSP00000481967.1:n.587-88C=
NM_000545.5:c.1382C= , LRG_522t1:c.1382C=	NP_000536.5:p.Pro461=
NM_000545.6:c.1382C=	NP_000536.5:p.Pro461=
NM_001306179.1:c.1382C=	NP_001293108.1:p.Pro461=
XM_005253931.2:c.1382C=	XP_005253988.1:p.Pro461=
XM_024449168.1:c.1382C=	XP_024304936.1:p.Pro461=
NM_000545.8:c.1382C= MANE Select	NP_000536.6:p.Pro461=
NM_001306179.2:c.1382C=	NP_001293108.2:p.Pro461=