Canonical Allele Identifier: CA771694970

Gene: HNF1B

Linked Data

• dbSNP Id: rs1235175491
• MyVariant Identifiers: chr17:g.37720544_37720545insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37720548dup , CM000679.2:g.37720548dup	GRCh38
NC_000017.10:g.36080543dup , CM000679.1:g.36080543dup	GRCh37
NC_000017.9:g.33154656dup	NCBI36
NG_013019.2:g.29562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.1046-9882dup MANE Select	ENSP00000480291.1:n.1046-9882dup
ENST00000613727.4:c.968-9882dup	ENSP00000477524.1:n.968-9882dup
ENST00000614313.4:c.1046-9882dup	ENSP00000482529.1:n.1046-9882dup
ENST00000617272.4:c.1046-9882dup	ENSP00000478682.1:n.1046-9882dup
ENST00000617811.4:c.1046-9882dup	ENSP00000480291.1:n.1046-9882dup
ENST00000621123.4:c.968-9882dup	ENSP00000482711.1:n.968-9882dup
NM_000458.3:c.1046-9882dup	NP_000449.1:n.1046-9882dup
NM_001165923.3:c.968-9882dup	NP_001159395.1:n.968-9882dup
NM_001304286.1:c.968-9882dup	NP_001291215.1:n.968-9882dup
XM_011525160.1:c.1046-9882dup	XP_011523462.1:n.1046-9882dup
XM_011525161.1:c.1046-9882dup	XP_011523463.1:n.1046-9882dup
XM_011525164.1:c.968-9882dup	XP_011523466.1:n.968-9882dup
XR_934718.1:n.2236-3317dup
XM_011525162.2:c.*302dup	XP_011523464.1:n.*302dup
XR_001752875.1:n.574+3062dup
NM_000458.4:c.1046-9882dup MANE Select	NP_000449.1:n.1046-9882dup
NM_001165923.4:c.968-9882dup	NP_001159395.1:n.968-9882dup
NM_001304286.2:c.968-9882dup	NP_001291215.1:n.968-9882dup