Canonical Allele Identifier: CA2575289359

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110342162del , CM000674.2:g.110342162del	GRCh38
NC_000012.11:g.110779967del , CM000674.1:g.110779967del	GRCh37
NC_000012.10:g.109264350del	NCBI36
NG_007097.2:g.65536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2098-66del MANE Select	ENSP00000440045.2:n.2098-66del
ENST00000308664.10:c.2098-66del	ENSP00000311186.6:n.2098-66del
ENST00000377685.9:c.*1938-66del	ENSP00000366913.4:n.*1938-66del
ENST00000539276.6:c.2098-66del	ENSP00000440045.2:n.2098-66del
ENST00000548169.2:c.1769-66del
NM_001681.3:c.2098-66del	NP_001672.1:n.2098-66del
NM_170665.3:c.2098-66del	NP_733765.1:n.2098-66del
XM_005253888.1:c.2098-66del	XP_005253945.1:n.2098-66del
XM_011538402.1:c.2098-66del	XP_011536704.1:n.2098-66del
XM_011538403.1:c.2098-66del	XP_011536705.1:n.2098-66del
XR_243009.1:n.2104-66del
XM_005253888.3:c.2098-66del	XP_005253945.1:n.2098-66del
XM_011538402.3:c.2098-66del	XP_011536704.1:n.2098-66del
XR_002957329.1:n.2104-66del
XR_243009.3:n.2104-66del
NM_170665.4:c.2098-66del MANE Select	NP_733765.1:n.2098-66del
NM_001681.4:c.2098-66del	NP_001672.1:n.2098-66del