Canonical Allele Identifier: CA2067683141

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120996361C= , CM000674.2:g.120996361C=	GRCh38
NC_000012.11:g.121434164C= , CM000674.1:g.121434164C=	GRCh37
NC_000012.10:g.119918547C=	NCBI36
NG_011731.2:g.22616C= , LRG_522:g.22616C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000545.8:c.1055C= MANE Select	NP_000536.6:p.Ser352=
ENST00000257555.11:c.1055C= MANE Select	ENSP00000257555.5:p.Ser352=
NM_000545.5:c.1055C= , LRG_522t1:c.1055C=	NP_000536.5:p.Ser352=
NM_000545.6:c.1055C=	NP_000536.5:p.Ser352=
NM_001306179.1:c.1055C=	NP_001293108.1:p.Ser352=
NM_001306179.2:c.1055C=	NP_001293108.2:p.Ser352=
ENST00000257555.10:c.1055C=	ENSP00000257555.4:p.Ser352=
ENST00000400024.6:c.1055C=	ENSP00000476181.1:p.Ser352=
ENST00000402929.5:n.1190C=
ENST00000535955.5:n.43-1130C=
ENST00000538626.2:n.191-1130C=
ENST00000538646.5:c.*31C=	ENSP00000443964.1:n.*31C=
ENST00000540108.1:c.*495C=	ENSP00000445445.1:n.*495C=
ENST00000541395.5:c.1055C=	ENSP00000443112.1:p.Ser352=
ENST00000541924.5:c.*69C=	ENSP00000440361.1:n.*69C=
ENST00000543427.5:c.634-243C=	ENSP00000439721.2:n.634-243C=
ENST00000544413.2:c.1055C=	ENSP00000438804.1:p.Ser352=
ENST00000544574.5:c.73-256C=	ENSP00000438565.1:n.73-256C=
ENST00000560968.5:c.894-22C=
ENST00000560968.6:c.751-22C=	ENSP00000453965.2:n.751-22C=
ENST00000615446.4:c.-158C=	ENSP00000483994.1:n.-158C=
ENST00000617366.4:c.587-1273C=	ENSP00000481967.1:n.587-1273C=
XM_005253931.2:c.1055C=	XP_005253988.1:p.Ser352=
XM_024449168.1:c.1055C=	XP_024304936.1:p.Ser352=