Canonical Allele Identifier: CA10650001

Gene: HNF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37686928T= , CM000679.2:g.37686928T=	GRCh38
NG_013019.2:g.63179A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.*444A= MANE Select	ENSP00000480291.1:n.*444A=
ENST00000617811.4:c.*444A=	ENSP00000480291.1:n.*444A=
NM_000458.3:c.*444A=	NP_000449.1:n.*444A=
NM_001165923.3:c.*444A=	NP_001159395.1:n.*444A=
NM_001304286.1:c.*352A=	NP_001291215.1:n.*352A=
XM_011525160.1:c.*352A=	XP_011523462.1:n.*352A=
XM_011525161.1:c.*444A=	XP_011523463.1:n.*444A=
XM_011525164.1:c.*352A=	XP_011523466.1:n.*352A=
XR_002958135.1:n.1273T=
NM_000458.4:c.*444A= MANE Select	NP_000449.1:n.*444A=
NM_001165923.4:c.*444A=	NP_001159395.1:n.*444A=
NM_001304286.2:c.*352A=	NP_001291215.1:n.*352A=