Canonical Allele Identifier: CA2258514332

Gene: HNF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37701316G= , CM000679.2:g.37701316G=	GRCh38
NC_000017.10:g.36061321G= , CM000679.1:g.36061321G=	GRCh37
NC_000017.9:g.33135434G=	NCBI36
NG_013019.2:g.48791C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.1340-139C= MANE Select	ENSP00000480291.1:n.1340-139C=
ENST00000613727.4:c.1261+3601C=	ENSP00000477524.1:n.1261+3601C=
ENST00000614313.4:c.1340-139C=	ENSP00000482529.1:n.1340-139C=
ENST00000617272.4:c.*63-139C=	ENSP00000478682.1:n.*63-139C=
ENST00000617811.4:c.1340-139C=	ENSP00000480291.1:n.1340-139C=
ENST00000621123.4:c.1262-139C=	ENSP00000482711.1:n.1262-139C=
NM_000458.3:c.1340-139C=	NP_000449.1:n.1340-139C=
NM_001165923.3:c.1262-139C=	NP_001159395.1:n.1262-139C=
NM_001304286.1:c.1261+3601C=	NP_001291215.1:n.1261+3601C=
XM_011525160.1:c.1340-139C=	XP_011523462.1:n.1340-139C=
XM_011525161.1:c.1340-2122C=	XP_011523463.1:n.1340-2122C=
XM_011525164.1:c.1262-139C=	XP_011523466.1:n.1262-139C=
NM_000458.4:c.1340-139C= MANE Select	NP_000449.1:n.1340-139C=
NM_001165923.4:c.1262-139C=	NP_001159395.1:n.1262-139C=
NM_001304286.2:c.1261+3601C=	NP_001291215.1:n.1261+3601C=