Canonical Allele Identifier: CA2637449517

Gene: HNF1B

Linked Data

• gnomAD v4: 17-37744905-A-ATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37744905_37744906insTTG , CM000679.2:g.37744905_37744906insTTG	GRCh38
NC_000017.10:g.36104896_36104897insTTG , CM000679.1:g.36104896_36104897insTTG	GRCh37
NC_000017.9:g.33179009_33179010insTTG	NCBI36
NG_013019.2:g.5201_5202insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.-22_-21insCAA MANE Select	ENSP00000480291.1:n.-22_-21insCAA
ENST00000613727.4:c.-22_-21insCAA	ENSP00000477524.1:n.-22_-21insCAA
ENST00000614313.4:c.-22_-21insCAA	ENSP00000482529.1:n.-22_-21insCAA
ENST00000617272.4:c.-22_-21insCAA	ENSP00000478682.1:n.-22_-21insCAA
ENST00000617811.4:c.-22_-21insCAA	ENSP00000480291.1:n.-22_-21insCAA
ENST00000620125.1:c.-22_-21insCAA	ENSP00000481245.1:n.-22_-21insCAA
ENST00000621123.4:c.-22_-21insCAA	ENSP00000482711.1:n.-22_-21insCAA
NM_000458.3:c.-22_-21insCAA	NP_000449.1:n.-22_-21insCAA
NM_001165923.3:c.-22_-21insCAA	NP_001159395.1:n.-22_-21insCAA
NM_001304286.1:c.-22_-21insCAA	NP_001291215.1:n.-22_-21insCAA
XM_011525160.1:c.-22_-21insCAA	XP_011523462.1:n.-22_-21insCAA
XM_011525161.1:c.-22_-21insCAA	XP_011523463.1:n.-22_-21insCAA
XM_011525162.1:c.-22_-21insCAA	XP_011523464.1:n.-22_-21insCAA
XM_011525163.1:c.-22_-21insCAA	XP_011523465.1:n.-22_-21insCAA
XM_011525164.1:c.-22_-21insCAA	XP_011523466.1:n.-22_-21insCAA
XM_011525162.2:c.-22_-21insCAA	XP_011523464.1:n.-22_-21insCAA
XM_011525163.2:c.-22_-21insCAA	XP_011523465.1:n.-22_-21insCAA
NM_000458.4:c.-22_-21insCAA MANE Select	NP_000449.1:n.-22_-21insCAA
NM_001165923.4:c.-22_-21insCAA	NP_001159395.1:n.-22_-21insCAA
NM_001304286.2:c.-22_-21insCAA	NP_001291215.1:n.-22_-21insCAA