Canonical Allele Identifier: CA383652502

Gene: ADIPOR2

Linked Data

• MyVariant Identifiers: chr12:g.1890101C>A (hg19) ; chr12:g.1780935C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780935C>A , CM000674.2:g.1780935C>A	GRCh38
NC_000012.11:g.1890101C>A , CM000674.1:g.1890101C>A	GRCh37
NC_000012.10:g.1760362C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357103.5:c.697C>A MANE Select	ENSP00000349616.4:p.Pro233Thr
ENST00000357103.4:c.697C>A	ENSP00000349616.4:p.Pro233Thr
ENST00000537190.1:n.537C>A
NM_024551.2:c.697C>A	NP_078827.2:p.Pro233Thr
XM_005253789.1:c.697C>A	XP_005253846.1:p.Pro233Thr
XM_006719018.1:c.697C>A	XP_006719081.1:p.Pro233Thr
XM_011521024.1:c.697C>A	XP_011519326.1:p.Pro233Thr
XM_011521025.1:c.463+2910C>A	XP_011519327.1:n.463+2910C>A
XM_005253789.2:c.697C>A	XP_005253846.1:p.Pro233Thr
XM_006719018.2:c.697C>A	XP_006719081.1:p.Pro233Thr
XM_011521024.2:c.697C>A	XP_011519326.1:p.Pro233Thr
NM_024551.3:c.697C>A MANE Select	NP_078827.2:p.Pro233Thr
NM_001375363.1:c.697C>A	NP_001362292.1:p.Pro233Thr
NM_001375364.1:c.697C>A	NP_001362293.1:p.Pro233Thr
NM_001375365.1:c.697C>A	NP_001362294.1:p.Pro233Thr