Canonical Allele Identifier: CA602890243

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs1269342122
• gnomAD v2: 12-1865995-TC-T
• gnomAD v3: 12-1756829-TC-T
• gnomAD v4: 12-1756829-TC-T
• MyVariant Identifiers: chr12:g.1865996del (hg19) ; chr12:g.1756830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1756830del , CM000674.2:g.1756830del	GRCh38
NC_000012.11:g.1865996del , CM000674.1:g.1865996del	GRCh37
NC_000012.10:g.1736257del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357103.5:c.171+2316del MANE Select	ENSP00000349616.4:n.171+2316del
ENST00000357103.4:c.171+2316del	ENSP00000349616.4:n.171+2316del
ENST00000537545.1:n.401+2316del
NM_024551.2:c.171+2316del	NP_078827.2:n.171+2316del
XM_005253789.1:c.171+2316del	XP_005253846.1:n.171+2316del
XM_006719018.1:c.171+2316del	XP_006719081.1:n.171+2316del
XM_011521024.1:c.171+2316del	XP_011519326.1:n.171+2316del
XM_011521025.1:c.171+2316del	XP_011519327.1:n.171+2316del
XM_005253789.2:c.171+2316del	XP_005253846.1:n.171+2316del
XM_006719018.2:c.171+2316del	XP_006719081.1:n.171+2316del
XM_011521024.2:c.171+2316del	XP_011519326.1:n.171+2316del
NM_024551.3:c.171+2316del MANE Select	NP_078827.2:n.171+2316del
NM_001375363.1:c.171+2316del	NP_001362292.1:n.171+2316del
NM_001375364.1:c.171+2316del	NP_001362293.1:n.171+2316del
NM_001375365.1:c.171+2316del	NP_001362294.1:n.171+2316del