Canonical Allele Identifier: CA602890240

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs1479122501
• gnomAD v2: 12-1865847-G-GT
• gnomAD v3: 12-1756681-G-GT
• gnomAD v4: 12-1756681-G-GT
• MyVariant Identifiers: chr12:g.1865847_1865848insT (hg19) ; chr12:g.1756681_1756682insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1756683dup , CM000674.2:g.1756683dup	GRCh38
NC_000012.11:g.1865849dup , CM000674.1:g.1865849dup	GRCh37
NC_000012.10:g.1736110dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357103.5:c.171+2169dup MANE Select	ENSP00000349616.4:n.171+2169dup
ENST00000357103.4:c.171+2169dup	ENSP00000349616.4:n.171+2169dup
ENST00000537545.1:n.401+2169dup
NM_024551.2:c.171+2169dup	NP_078827.2:n.171+2169dup
XM_005253789.1:c.171+2169dup	XP_005253846.1:n.171+2169dup
XM_006719018.1:c.171+2169dup	XP_006719081.1:n.171+2169dup
XM_011521024.1:c.171+2169dup	XP_011519326.1:n.171+2169dup
XM_011521025.1:c.171+2169dup	XP_011519327.1:n.171+2169dup
XM_005253789.2:c.171+2169dup	XP_005253846.1:n.171+2169dup
XM_006719018.2:c.171+2169dup	XP_006719081.1:n.171+2169dup
XM_011521024.2:c.171+2169dup	XP_011519326.1:n.171+2169dup
NM_024551.3:c.171+2169dup MANE Select	NP_078827.2:n.171+2169dup
NM_001375363.1:c.171+2169dup	NP_001362292.1:n.171+2169dup
NM_001375364.1:c.171+2169dup	NP_001362293.1:n.171+2169dup
NM_001375365.1:c.171+2169dup	NP_001362294.1:n.171+2169dup