Canonical Allele Identifier: CA2067682927

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996272T= , CM000674.2:g.120996272T=	GRCh38
NC_000012.11:g.121434075T= , CM000674.1:g.121434075T=	GRCh37
NC_000012.10:g.119918458T=	NCBI36
NG_011731.2:g.22527T= , LRG_522:g.22527T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.751-111T=	ENSP00000453965.2:n.751-111T=
ENST00000257555.11:c.966T= MANE Select	ENSP00000257555.5:p.Tyr322=
ENST00000257555.10:c.966T=	ENSP00000257555.4:p.Tyr322=
ENST00000400024.6:c.966T=	ENSP00000476181.1:p.Tyr322=
ENST00000402929.5:n.1101T=
ENST00000535955.5:n.43-1219T=
ENST00000538626.2:n.191-1219T=
ENST00000538646.5:c.779T=	ENSP00000443964.1:p.Met260=
ENST00000540108.1:c.*406T=	ENSP00000445445.1:n.*406T=
ENST00000541395.5:c.966T=	ENSP00000443112.1:p.Tyr322=
ENST00000541924.5:c.724T=	ENSP00000440361.1:p.Trp242=
ENST00000543427.5:c.634-332T=	ENSP00000439721.2:n.634-332T=
ENST00000544413.2:c.966T=	ENSP00000438804.1:p.Tyr322=
ENST00000544574.5:c.73-345T=	ENSP00000438565.1:n.73-345T=
ENST00000560968.5:c.894-111T=
ENST00000615446.4:c.-247T=	ENSP00000483994.1:n.-247T=
ENST00000617366.4:c.587-1362T=	ENSP00000481967.1:n.587-1362T=
NM_000545.5:c.966T= , LRG_522t1:c.966T=	NP_000536.5:p.Tyr322=
NM_000545.6:c.966T=	NP_000536.5:p.Tyr322=
NM_001306179.1:c.966T=	NP_001293108.1:p.Tyr322=
XM_005253931.2:c.966T=	XP_005253988.1:p.Tyr322=
XM_024449168.1:c.966T=	XP_024304936.1:p.Tyr322=
NM_000545.8:c.966T= MANE Select	NP_000536.6:p.Tyr322=
NM_001306179.2:c.966T=	NP_001293108.2:p.Tyr322=