Canonical Allele Identifier: CA2067678502

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120993686G= , CM000674.2:g.120993686G=	GRCh38
NC_000012.11:g.121431489G= , CM000674.1:g.121431489G=	GRCh37
NC_000012.10:g.119915872G=	NCBI36
NG_011731.2:g.19941G= , LRG_522:g.19941G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.693G=	ENSP00000453965.2:p.Thr231=
ENST00000257555.11:c.693G= MANE Select	ENSP00000257555.5:p.Thr231=
ENST00000257555.10:c.693G=	ENSP00000257555.4:p.Thr231=
ENST00000400024.6:c.693G=	ENSP00000476181.1:p.Thr231=
ENST00000402929.5:n.828G=
ENST00000535955.5:n.43-3805G=
ENST00000538626.2:n.191-3805G=
ENST00000538646.5:c.527-478G=	ENSP00000443964.1:n.527-478G=
ENST00000540108.1:c.*133G=	ENSP00000445445.1:n.*133G=
ENST00000541395.5:c.693G=	ENSP00000443112.1:p.Thr231=
ENST00000541924.5:c.693G=	ENSP00000440361.1:p.Thr231=
ENST00000543427.5:c.633+60G=	ENSP00000439721.2:n.633+60G=
ENST00000544413.2:c.693G=	ENSP00000438804.1:p.Thr231=
ENST00000544574.5:c.73-2931G=	ENSP00000438565.1:n.73-2931G=
ENST00000560968.5:c.836G=
ENST00000615446.4:c.-257-2576G=	ENSP00000483994.1:n.-257-2576G=
ENST00000617366.4:c.586+107G=	ENSP00000481967.1:n.586+107G=
NM_000545.5:c.693G= , LRG_522t1:c.693G=	NP_000536.5:p.Thr231=
NM_000545.6:c.693G=	NP_000536.5:p.Thr231=
NM_001306179.1:c.693G=	NP_001293108.1:p.Thr231=
XM_005253931.2:c.693G=	XP_005253988.1:p.Thr231=
XM_024449168.1:c.693G=	XP_024304936.1:p.Thr231=
NM_000545.8:c.693G= MANE Select	NP_000536.6:p.Thr231=
NM_001306179.2:c.693G=	NP_001293108.2:p.Thr231=