Canonical Allele Identifier: CA386676177

Gene: ATP2A2

Linked Data

• MyVariant Identifiers: chr12:g.110781166G>C (hg19) ; chr12:g.110343361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110343361G>C , CM000674.2:g.110343361G>C	GRCh38
NC_000012.11:g.110781166G>C , CM000674.1:g.110781166G>C	GRCh37
NC_000012.10:g.109265549G>C	NCBI36
NG_007097.2:g.66735G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2448G>C MANE Select	ENSP00000440045.2:p.Met816Ile
ENST00000308664.10:c.2448G>C	ENSP00000311186.6:p.Met816Ile
ENST00000377685.9:c.*2288G>C	ENSP00000366913.4:n.*2288G>C
ENST00000539276.6:c.2448G>C	ENSP00000440045.2:p.Met816Ile
ENST00000547792.1:n.106G>C
ENST00000548169.2:c.2119G>C
NM_001681.3:c.2448G>C	NP_001672.1:p.Met816Ile
NM_170665.3:c.2448G>C	NP_733765.1:p.Met816Ile
XM_005253888.1:c.2448G>C	XP_005253945.1:p.Met816Ile
XM_011538402.1:c.2448G>C	XP_011536704.1:p.Met816Ile
XM_011538403.1:c.2448G>C	XP_011536705.1:p.Met816Ile
XR_243009.1:n.2454G>C
XM_005253888.3:c.2448G>C	XP_005253945.1:p.Met816Ile
XM_011538402.3:c.2448G>C	XP_011536704.1:p.Met816Ile
XR_002957329.1:n.2454G>C
XR_243009.3:n.2454G>C
NM_170665.4:c.2448G>C MANE Select	NP_733765.1:p.Met816Ile
NM_001681.4:c.2448G>C	NP_001672.1:p.Met816Ile