Canonical Allele Identifier: CA2062809660

Gene: ATP2A2

Linked Data

• dbSNP Id: rs1879722243

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345155_110345156insCTG , CM000674.2:g.110345155_110345156insCTG	GRCh38
NC_000012.11:g.110782960_110782961insCTG , CM000674.1:g.110782960_110782961insCTG	GRCh37
NC_000012.10:g.109267343_109267344insCTG	NCBI36
NG_007097.2:g.68529_68530insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2608-94_2608-93insCTG MANE Select	ENSP00000440045.2:n.2608-94_2608-93insCTG
ENST00000308664.10:c.2608-94_2608-93insCTG	ENSP00000311186.6:n.2608-94_2608-93insCTG
ENST00000377685.9:c.*2448-94_*2448-93insCTG	ENSP00000366913.4:n.*2448-94_*2448-93insCTG
ENST00000539276.6:c.2608-94_2608-93insCTG	ENSP00000440045.2:n.2608-94_2608-93insCTG
ENST00000547792.1:n.449_450insCTG
ENST00000548169.2:c.2279-94_2279-93insCTG
NM_001681.3:c.2608-94_2608-93insCTG	NP_001672.1:n.2608-94_2608-93insCTG
NM_170665.3:c.2608-94_2608-93insCTG	NP_733765.1:n.2608-94_2608-93insCTG
XM_005253888.1:c.2608-94_2608-93insCTG	XP_005253945.1:n.2608-94_2608-93insCTG
XM_011538402.1:c.2608-94_2608-93insCTG	XP_011536704.1:n.2608-94_2608-93insCTG
XR_243009.1:n.2614-94_2614-93insCTG
XM_005253888.3:c.2608-94_2608-93insCTG	XP_005253945.1:n.2608-94_2608-93insCTG
XM_011538402.3:c.2608-94_2608-93insCTG	XP_011536704.1:n.2608-94_2608-93insCTG
XR_002957329.1:n.2614-94_2614-93insCTG
XR_243009.3:n.2614-94_2614-93insCTG
NM_170665.4:c.2608-94_2608-93insCTG MANE Select	NP_733765.1:n.2608-94_2608-93insCTG
NM_001681.4:c.2608-94_2608-93insCTG	NP_001672.1:n.2608-94_2608-93insCTG