Canonical Allele Identifier: CA2062806310

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110342457_110342459delinsCTG , CM000674.2:g.110342457_110342459delinsCTG	GRCh38
NC_000012.11:g.110780262_110780264delinsCTG , CM000674.1:g.110780262_110780264delinsCTG	GRCh37
NC_000012.10:g.109264645_109264647delinsCTG	NCBI36
NG_007097.2:g.65831_65833delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2318+9_2318+11delinsCTG MANE Select	ENSP00000440045.2:n.2318+9_2318+11delinsCTG
ENST00000308664.10:c.2318+9_2318+11delinsCTG	ENSP00000311186.6:n.2318+9_2318+11delinsCTG
ENST00000377685.9:c.*2158+9_*2158+11delinsCTG	ENSP00000366913.4:n.*2158+9_*2158+11delinsCTG
ENST00000539276.6:c.2318+9_2318+11delinsCTG	ENSP00000440045.2:n.2318+9_2318+11delinsCTG
ENST00000548169.2:c.1989+9_1989+11delinsCTG
NM_001681.3:c.2318+9_2318+11delinsCTG	NP_001672.1:n.2318+9_2318+11delinsCTG
NM_170665.3:c.2318+9_2318+11delinsCTG	NP_733765.1:n.2318+9_2318+11delinsCTG
XM_005253888.1:c.2318+9_2318+11delinsCTG	XP_005253945.1:n.2318+9_2318+11delinsCTG
XM_011538402.1:c.2318+9_2318+11delinsCTG	XP_011536704.1:n.2318+9_2318+11delinsCTG
XM_011538403.1:c.2318+9_2318+11delinsCTG	XP_011536705.1:n.2318+9_2318+11delinsCTG
XR_243009.1:n.2324+9_2324+11delinsCTG
XM_005253888.3:c.2318+9_2318+11delinsCTG	XP_005253945.1:n.2318+9_2318+11delinsCTG
XM_011538402.3:c.2318+9_2318+11delinsCTG	XP_011536704.1:n.2318+9_2318+11delinsCTG
XR_002957329.1:n.2324+9_2324+11delinsCTG
XR_243009.3:n.2324+9_2324+11delinsCTG
NM_170665.4:c.2318+9_2318+11delinsCTG MANE Select	NP_733765.1:n.2318+9_2318+11delinsCTG
NM_001681.4:c.2318+9_2318+11delinsCTG	NP_001672.1:n.2318+9_2318+11delinsCTG