Canonical Allele Identifier: CA2067666718

Gene: HNF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120983040C= , CM000674.2:g.120983040C=	GRCh38
NC_000012.11:g.121420843C= , CM000674.1:g.121420843C=	GRCh37
NC_000012.10:g.119905226C=	NCBI36
NG_011731.2:g.9295C= , LRG_522:g.9295C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000560968.6:c.326+3946C=	ENSP00000453965.2:n.326+3946C=
ENST00000257555.11:c.326+3946C= MANE Select	ENSP00000257555.5:n.326+3946C=
ENST00000257555.10:c.326+3946C=	ENSP00000257555.4:n.326+3946C=
ENST00000400024.6:c.326+3946C=	ENSP00000476181.1:n.326+3946C=
ENST00000402929.5:n.461+3946C=
ENST00000535955.5:n.42+4348C=
ENST00000538626.2:n.190+4200C=
ENST00000538646.5:c.326+3946C=	ENSP00000443964.1:n.326+3946C=
ENST00000540108.1:c.326+3946C=	ENSP00000445445.1:n.326+3946C=
ENST00000541395.5:c.326+3946C=	ENSP00000443112.1:n.326+3946C=
ENST00000541924.5:c.326+3946C=	ENSP00000440361.1:n.326+3946C=
ENST00000543427.5:c.326+3946C=	ENSP00000439721.2:n.326+3946C=
ENST00000544413.2:c.326+3946C=	ENSP00000438804.1:n.326+3946C=
ENST00000544574.5:c.72+4200C=	ENSP00000438565.1:n.72+4200C=
ENST00000560968.5:c.469+3946C=
ENST00000615446.4:c.-258+4329C=	ENSP00000483994.1:n.-258+4329C=
ENST00000617366.4:c.326+3946C=	ENSP00000481967.1:n.326+3946C=
NM_000545.5:c.326+3946C= , LRG_522t1:c.326+3946C=	NP_000536.5:n.326+3946C=
NM_000545.6:c.326+3946C=	NP_000536.5:n.326+3946C=
NM_001306179.1:c.326+3946C=	NP_001293108.1:n.326+3946C=
XM_005253931.2:c.326+3946C=	XP_005253988.1:n.326+3946C=
XM_024449168.1:c.326+3946C=	XP_024304936.1:n.326+3946C=
NM_000545.8:c.326+3946C= MANE Select	NP_000536.6:n.326+3946C=
NM_001306179.2:c.326+3946C=	NP_001293108.2:n.326+3946C=