Canonical Allele Identifier: CA771694924

Gene: HNF1B

Linked Data

• dbSNP Id: rs1168653075
• MyVariant Identifiers: chr17:g.37720498_37720499insTTATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37720500_37720504dup , CM000679.2:g.37720500_37720504dup	GRCh38
NC_000017.10:g.36080495_36080499dup , CM000679.1:g.36080495_36080499dup	GRCh37
NC_000017.9:g.33154608_33154612dup	NCBI36
NG_013019.2:g.29604_29608dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.1046-9840_1046-9836dup MANE Select	ENSP00000480291.1:n.1046-9840_1046-9836du...
ENST00000613727.4:c.968-9840_968-9836dup	ENSP00000477524.1:n.968-9840_968-9836dup
ENST00000614313.4:c.1046-9840_1046-9836dup	ENSP00000482529.1:n.1046-9840_1046-9836du...
ENST00000617272.4:c.1046-9840_1046-9836dup	ENSP00000478682.1:n.1046-9840_1046-9836du...
ENST00000617811.4:c.1046-9840_1046-9836dup	ENSP00000480291.1:n.1046-9840_1046-9836du...
ENST00000621123.4:c.968-9840_968-9836dup	ENSP00000482711.1:n.968-9840_968-9836dup
NM_000458.3:c.1046-9840_1046-9836dup	NP_000449.1:n.1046-9840_1046-9836dup
NM_001165923.3:c.968-9840_968-9836dup	NP_001159395.1:n.968-9840_968-9836dup
NM_001304286.1:c.968-9840_968-9836dup	NP_001291215.1:n.968-9840_968-9836dup
XM_011525160.1:c.1046-9840_1046-9836dup	XP_011523462.1:n.1046-9840_1046-9836dup
XM_011525161.1:c.1046-9840_1046-9836dup	XP_011523463.1:n.1046-9840_1046-9836dup
XM_011525164.1:c.968-9840_968-9836dup	XP_011523466.1:n.968-9840_968-9836dup
XR_934718.1:n.2236-3365_2236-3361dup
XM_011525162.2:c.*344_*348dup	XP_011523464.1:n.*344_*348dup
XR_001752875.1:n.574+3014_574+3018dup
NM_000458.4:c.1046-9840_1046-9836dup MANE Select	NP_000449.1:n.1046-9840_1046-9836dup
NM_001165923.4:c.968-9840_968-9836dup	NP_001159395.1:n.968-9840_968-9836dup
NM_001304286.2:c.968-9840_968-9836dup	NP_001291215.1:n.968-9840_968-9836dup