Canonical Allele Identifier: CA2062807129

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110343370_110343371delinsTC , CM000674.2:g.110343370_110343371delinsTC	GRCh38
NC_000012.11:g.110781175_110781176delinsTC , CM000674.1:g.110781175_110781176delinsTC	GRCh37
NC_000012.10:g.109265558_109265559delinsTC	NCBI36
NG_007097.2:g.66744_66745delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2457_2458delinsTC MANE Select	ENSP00000440045.2:p.Pro819=
ENST00000308664.10:c.2457_2458delinsTC	ENSP00000311186.6:p.Pro819=
ENST00000377685.9:c.*2297_*2298delinsTC	ENSP00000366913.4:n.*2297_*2298delinsTC
ENST00000539276.6:c.2457_2458delinsTC	ENSP00000440045.2:p.Pro819=
ENST00000547792.1:n.115_116delinsTC
ENST00000548169.2:c.2128_2129delinsTC
NM_001681.3:c.2457_2458delinsTC	NP_001672.1:p.Pro819=
NM_170665.3:c.2457_2458delinsTC	NP_733765.1:p.Pro819=
XM_005253888.1:c.2457_2458delinsTC	XP_005253945.1:p.Pro819=
XM_011538402.1:c.2457_2458delinsTC	XP_011536704.1:p.Pro819=
XM_011538403.1:c.2457_2458delinsTC	XP_011536705.1:p.Pro819=
XR_243009.1:n.2463_2464delinsTC
XM_005253888.3:c.2457_2458delinsTC	XP_005253945.1:p.Pro819=
XM_011538402.3:c.2457_2458delinsTC	XP_011536704.1:p.Pro819=
XR_002957329.1:n.2463_2464delinsTC
XR_243009.3:n.2463_2464delinsTC
NM_170665.4:c.2457_2458delinsTC MANE Select	NP_733765.1:p.Pro819=
NM_001681.4:c.2457_2458delinsTC	NP_001672.1:p.Pro819=