Canonical Allele Identifier: CA386677472

Gene: ATP2A2

Linked Data

• MyVariant Identifiers: chr12:g.110783141G>T (hg19) ; chr12:g.110345336G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345336G>T , CM000674.2:g.110345336G>T	GRCh38
NC_000012.11:g.110783141G>T , CM000674.1:g.110783141G>T	GRCh37
NC_000012.10:g.109267524G>T	NCBI36
NG_007097.2:g.68710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2695G>T MANE Select	ENSP00000440045.2:p.Ala899Ser
ENST00000308664.10:c.2695G>T	ENSP00000311186.6:p.Ala899Ser
ENST00000377685.9:c.*2535G>T	ENSP00000366913.4:n.*2535G>T
ENST00000539276.6:c.2695G>T	ENSP00000440045.2:p.Ala899Ser
ENST00000548169.2:c.2366G>T
NM_001681.3:c.2695G>T	NP_001672.1:p.Ala899Ser
NM_170665.3:c.2695G>T	NP_733765.1:p.Ala899Ser
XM_005253888.1:c.2695G>T	XP_005253945.1:p.Ala899Ser
XM_011538402.1:c.2695G>T	XP_011536704.1:p.Ala899Ser
XR_243009.1:n.2701G>T
XM_005253888.3:c.2695G>T	XP_005253945.1:p.Ala899Ser
XM_011538402.3:c.2695G>T	XP_011536704.1:p.Ala899Ser
XR_002957329.1:n.2701G>T
XR_243009.3:n.2701G>T
NM_170665.4:c.2695G>T MANE Select	NP_733765.1:p.Ala899Ser
NM_001681.4:c.2695G>T	NP_001672.1:p.Ala899Ser