Canonical Allele Identifier: CA290273504

Gene: HNF1B

Linked Data

• dbSNP Id: rs754776125
• gnomAD v2: 17-36080503-C-CAT
• gnomAD v3: 17-37720508-C-CAT
• gnomAD v4: 17-37720508-C-CAT
• MyVariant Identifiers: chr17:g.36080505_36080506insAT (hg19) ; chr17:g.36080503_36080504insAT (hg19) ; chr17:g.37720510_37720511insAT (hg38) ; chr17:g.37720508_37720509insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37720518_37720519dup , CM000679.2:g.37720518_37720519dup	GRCh38
NC_000017.10:g.36080513_36080514dup , CM000679.1:g.36080513_36080514dup	GRCh37
NC_000017.9:g.33154626_33154627dup	NCBI36
NG_013019.2:g.29597_29598dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.1046-9847_1046-9846dup MANE Select	ENSP00000480291.1:n.1046-9847_1046-9846du...
ENST00000613727.4:c.968-9847_968-9846dup	ENSP00000477524.1:n.968-9847_968-9846dup
ENST00000614313.4:c.1046-9847_1046-9846dup	ENSP00000482529.1:n.1046-9847_1046-9846du...
ENST00000617272.4:c.1046-9847_1046-9846dup	ENSP00000478682.1:n.1046-9847_1046-9846du...
ENST00000617811.4:c.1046-9847_1046-9846dup	ENSP00000480291.1:n.1046-9847_1046-9846du...
ENST00000621123.4:c.968-9847_968-9846dup	ENSP00000482711.1:n.968-9847_968-9846dup
NM_000458.3:c.1046-9847_1046-9846dup	NP_000449.1:n.1046-9847_1046-9846dup
NM_001165923.3:c.968-9847_968-9846dup	NP_001159395.1:n.968-9847_968-9846dup
NM_001304286.1:c.968-9847_968-9846dup	NP_001291215.1:n.968-9847_968-9846dup
XM_011525160.1:c.1046-9847_1046-9846dup	XP_011523462.1:n.1046-9847_1046-9846dup
XM_011525161.1:c.1046-9847_1046-9846dup	XP_011523463.1:n.1046-9847_1046-9846dup
XM_011525164.1:c.968-9847_968-9846dup	XP_011523466.1:n.968-9847_968-9846dup
XR_934718.1:n.2236-3347_2236-3346dup
XM_011525162.2:c.*337_*338dup	XP_011523464.1:n.*337_*338dup
XR_001752875.1:n.574+3032_574+3033dup
NM_000458.4:c.1046-9847_1046-9846dup MANE Select	NP_000449.1:n.1046-9847_1046-9846dup
NM_001165923.4:c.968-9847_968-9846dup	NP_001159395.1:n.968-9847_968-9846dup
NM_001304286.2:c.968-9847_968-9846dup	NP_001291215.1:n.968-9847_968-9846dup