Canonical Allele Identifier: CA383652258

Gene: ADIPOR2

Linked Data

• MyVariant Identifiers: chr12:g.1889745T>A (hg19) ; chr12:g.1780579T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780579T>A , CM000674.2:g.1780579T>A	GRCh38
NC_000012.11:g.1889745T>A , CM000674.1:g.1889745T>A	GRCh37
NC_000012.10:g.1760006T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.592T>A MANE Select	ENSP00000349616.4:p.Ser198Thr
ENST00000357103.4:c.592T>A	ENSP00000349616.4:p.Ser198Thr
ENST00000537190.1:n.432T>A
NM_024551.2:c.592T>A	NP_078827.2:p.Ser198Thr
XM_005253789.1:c.592T>A	XP_005253846.1:p.Ser198Thr
XM_006719018.1:c.592T>A	XP_006719081.1:p.Ser198Thr
XM_011521024.1:c.592T>A	XP_011519326.1:p.Ser198Thr
XM_011521025.1:c.463+2554T>A	XP_011519327.1:n.463+2554T>A
XM_005253789.2:c.592T>A	XP_005253846.1:p.Ser198Thr
XM_006719018.2:c.592T>A	XP_006719081.1:p.Ser198Thr
XM_011521024.2:c.592T>A	XP_011519326.1:p.Ser198Thr
NM_024551.3:c.592T>A MANE Select	NP_078827.2:p.Ser198Thr
NM_001375363.1:c.592T>A	NP_001362292.1:p.Ser198Thr
NM_001375364.1:c.592T>A	NP_001362293.1:p.Ser198Thr
NM_001375365.1:c.592T>A	NP_001362294.1:p.Ser198Thr