Canonical Allele Identifier: CA2062807551

Gene: ATP2A2

Linked Data

• dbSNP Id: rs1879571545

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110343667_110343670del , CM000674.2:g.110343667_110343670del	GRCh38
NC_000012.11:g.110781472_110781475del , CM000674.1:g.110781472_110781475del	GRCh37
NC_000012.10:g.109265855_109265858del	NCBI36
NG_007097.2:g.67041_67044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2521+233_2521+236del MANE Select	ENSP00000440045.2:n.2521+233_2521+236del
ENST00000308664.10:c.2521+233_2521+236del	ENSP00000311186.6:n.2521+233_2521+236del
ENST00000377685.9:c.*2361+233_*2361+236del	ENSP00000366913.4:n.*2361+233_*2361+236del
ENST00000539276.6:c.2521+233_2521+236del	ENSP00000440045.2:n.2521+233_2521+236del
ENST00000547792.1:n.179+233_179+236del
ENST00000548169.2:c.2192+233_2192+236del
NM_001681.3:c.2521+233_2521+236del	NP_001672.1:n.2521+233_2521+236del
NM_170665.3:c.2521+233_2521+236del	NP_733765.1:n.2521+233_2521+236del
XM_005253888.1:c.2521+233_2521+236del	XP_005253945.1:n.2521+233_2521+236del
XM_011538402.1:c.2521+233_2521+236del	XP_011536704.1:n.2521+233_2521+236del
XM_011538403.1:c.2521+233_2521+236del	XP_011536705.1:n.2521+233_2521+236del
XR_243009.1:n.2527+233_2527+236del
XM_005253888.3:c.2521+233_2521+236del	XP_005253945.1:n.2521+233_2521+236del
XM_011538402.3:c.2521+233_2521+236del	XP_011536704.1:n.2521+233_2521+236del
XR_002957329.1:n.2527+233_2527+236del
XR_243009.3:n.2527+233_2527+236del
NM_170665.4:c.2521+233_2521+236del MANE Select	NP_733765.1:n.2521+233_2521+236del
NM_001681.4:c.2521+233_2521+236del	NP_001672.1:n.2521+233_2521+236del