Canonical Allele Identifier: CA2062807550
Gene: ATP2A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110343664_110343668delinsCAATT , CM000674.2:g.110343664_110343668delinsCAATT GRCh38
NC_000012.11:g.110781469_110781473delinsCAATT , CM000674.1:g.110781469_110781473delinsCAATT GRCh37
NC_000012.10:g.109265852_109265856delinsCAATT NCBI36
NG_007097.2:g.67038_67042delinsCAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.2521+230_2521+234delinsCAATT MANE Select ENSP00000440045.2:n.2521+230_2521+234delinsCAATT
ENST00000308664.10:c.2521+230_2521+234delinsCAATT ENSP00000311186.6:n.2521+230_2521+234delinsCAATT
ENST00000377685.9:c.*2361+230_*2361+234delinsCAATT ENSP00000366913.4:n.*2361+230_*2361+234delinsCAATT
ENST00000539276.6:c.2521+230_2521+234delinsCAATT ENSP00000440045.2:n.2521+230_2521+234delinsCAATT
ENST00000547792.1:n.179+230_179+234delinsCAATT
ENST00000548169.2:c.2192+230_2192+234delinsCAATT
NM_001681.3:c.2521+230_2521+234delinsCAATT NP_001672.1:n.2521+230_2521+234delinsCAATT
NM_170665.3:c.2521+230_2521+234delinsCAATT NP_733765.1:n.2521+230_2521+234delinsCAATT
XM_005253888.1:c.2521+230_2521+234delinsCAATT XP_005253945.1:n.2521+230_2521+234delinsCAATT
XM_011538402.1:c.2521+230_2521+234delinsCAATT XP_011536704.1:n.2521+230_2521+234delinsCAATT
XM_011538403.1:c.2521+230_2521+234delinsCAATT XP_011536705.1:n.2521+230_2521+234delinsCAATT
XR_243009.1:n.2527+230_2527+234delinsCAATT
XM_005253888.3:c.2521+230_2521+234delinsCAATT XP_005253945.1:n.2521+230_2521+234delinsCAATT
XM_011538402.3:c.2521+230_2521+234delinsCAATT XP_011536704.1:n.2521+230_2521+234delinsCAATT
XR_002957329.1:n.2527+230_2527+234delinsCAATT
XR_243009.3:n.2527+230_2527+234delinsCAATT
NM_170665.4:c.2521+230_2521+234delinsCAATT MANE Select NP_733765.1:n.2521+230_2521+234delinsCAATT
NM_001681.4:c.2521+230_2521+234delinsCAATT NP_001672.1:n.2521+230_2521+234delinsCAATT