Canonical Allele Identifier: CA383652269

Gene: ADIPOR2

Linked Data

• gnomAD v4: 12-1780584-G-C
• MyVariant Identifiers: chr12:g.1889750G>C (hg19) ; chr12:g.1780584G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780584G>C , CM000674.2:g.1780584G>C	GRCh38
NC_000012.11:g.1889750G>C , CM000674.1:g.1889750G>C	GRCh37
NC_000012.10:g.1760011G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.597G>C MANE Select	ENSP00000349616.4:p.Trp199Cys
ENST00000357103.4:c.597G>C	ENSP00000349616.4:p.Trp199Cys
ENST00000537190.1:n.437G>C
NM_024551.2:c.597G>C	NP_078827.2:p.Trp199Cys
XM_005253789.1:c.597G>C	XP_005253846.1:p.Trp199Cys
XM_006719018.1:c.597G>C	XP_006719081.1:p.Trp199Cys
XM_011521024.1:c.597G>C	XP_011519326.1:p.Trp199Cys
XM_011521025.1:c.463+2559G>C	XP_011519327.1:n.463+2559G>C
XM_005253789.2:c.597G>C	XP_005253846.1:p.Trp199Cys
XM_006719018.2:c.597G>C	XP_006719081.1:p.Trp199Cys
XM_011521024.2:c.597G>C	XP_011519326.1:p.Trp199Cys
NM_024551.3:c.597G>C MANE Select	NP_078827.2:p.Trp199Cys
NM_001375363.1:c.597G>C	NP_001362292.1:p.Trp199Cys
NM_001375364.1:c.597G>C	NP_001362293.1:p.Trp199Cys
NM_001375365.1:c.597G>C	NP_001362294.1:p.Trp199Cys