Canonical Allele Identifier: CA2067679091

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120994105G= , CM000674.2:g.120994105G=	GRCh38
NC_000012.11:g.121431908G= , CM000674.1:g.121431908G=	GRCh37
NC_000012.10:g.119916291G=	NCBI36
NG_011731.2:g.20360G= , LRG_522:g.20360G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560968.6:c.714-59G=	ENSP00000453965.2:n.714-59G=
ENST00000257555.11:c.714-59G= MANE Select	ENSP00000257555.5:n.714-59G=
ENST00000257555.10:c.714-59G=	ENSP00000257555.4:n.714-59G=
ENST00000400024.6:c.714-59G=	ENSP00000476181.1:n.714-59G=
ENST00000402929.5:n.849-59G=
ENST00000535955.5:n.43-3386G=
ENST00000538626.2:n.191-3386G=
ENST00000538646.5:c.527-59G=	ENSP00000443964.1:n.527-59G=
ENST00000540108.1:c.*154-59G=	ENSP00000445445.1:n.*154-59G=
ENST00000541395.5:c.714-59G=	ENSP00000443112.1:n.714-59G=
ENST00000541924.5:c.713+399G=	ENSP00000440361.1:n.713+399G=
ENST00000543427.5:c.633+479G=	ENSP00000439721.2:n.633+479G=
ENST00000544413.2:c.714-59G=	ENSP00000438804.1:n.714-59G=
ENST00000544574.5:c.73-2512G=	ENSP00000438565.1:n.73-2512G=
ENST00000560968.5:c.857-59G=
ENST00000615446.4:c.-257-2157G=	ENSP00000483994.1:n.-257-2157G=
ENST00000617366.4:c.586+526G=	ENSP00000481967.1:n.586+526G=
NM_000545.5:c.714-59G= , LRG_522t1:c.714-59G=	NP_000536.5:n.714-59G=
NM_000545.6:c.714-59G=	NP_000536.5:n.714-59G=
NM_001306179.1:c.714-59G=	NP_001293108.1:n.714-59G=
XM_005253931.2:c.714-59G=	XP_005253988.1:n.714-59G=
XM_024449168.1:c.714-59G=	XP_024304936.1:n.714-59G=
NM_000545.8:c.714-59G= MANE Select	NP_000536.6:n.714-59G=
NM_001306179.2:c.714-59G=	NP_001293108.2:n.714-59G=