Canonical Allele Identifier: CA386677465

Gene: ATP2A2

Linked Data

• MyVariant Identifiers: chr12:g.110783139T>A (hg19) ; chr12:g.110345334T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345334T>A , CM000674.2:g.110345334T>A	GRCh38
NC_000012.11:g.110783139T>A , CM000674.1:g.110783139T>A	GRCh37
NC_000012.10:g.109267522T>A	NCBI36
NG_007097.2:g.68708T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2693T>A MANE Select	ENSP00000440045.2:p.Met898Lys
ENST00000308664.10:c.2693T>A	ENSP00000311186.6:p.Met898Lys
ENST00000377685.9:c.*2533T>A	ENSP00000366913.4:n.*2533T>A
ENST00000539276.6:c.2693T>A	ENSP00000440045.2:p.Met898Lys
ENST00000548169.2:c.2364T>A
NM_001681.3:c.2693T>A	NP_001672.1:p.Met898Lys
NM_170665.3:c.2693T>A	NP_733765.1:p.Met898Lys
XM_005253888.1:c.2693T>A	XP_005253945.1:p.Met898Lys
XM_011538402.1:c.2693T>A	XP_011536704.1:p.Met898Lys
XR_243009.1:n.2699T>A
XM_005253888.3:c.2693T>A	XP_005253945.1:p.Met898Lys
XM_011538402.3:c.2693T>A	XP_011536704.1:p.Met898Lys
XR_002957329.1:n.2699T>A
XR_243009.3:n.2699T>A
NM_170665.4:c.2693T>A MANE Select	NP_733765.1:p.Met898Lys
NM_001681.4:c.2693T>A	NP_001672.1:p.Met898Lys