Canonical Allele Identifier: CA2062803192
Gene: ATP2A2 HGNC NCBI

Linked Data

dbSNP Id: rs1879125718

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110339215_110339216insA , CM000674.2:g.110339215_110339216insA GRCh38
NC_000012.11:g.110777020_110777021insA , CM000674.1:g.110777020_110777021insA GRCh37
NC_000012.10:g.109261403_109261404insA NCBI36
NG_007097.2:g.62589_62590insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000539276.7:c.1420-66_1420-65insA MANE Select ENSP00000440045.2:n.1420-66_1420-65insA
ENST00000308664.10:c.1420-66_1420-65insA ENSP00000311186.6:n.1420-66_1420-65insA
ENST00000377685.9:c.*1260-66_*1260-65insA ENSP00000366913.4:n.*1260-66_*1260-65insA
ENST00000539276.6:c.1420-66_1420-65insA ENSP00000440045.2:n.1420-66_1420-65insA
ENST00000548169.2:c.1091-66_1091-65insA
NM_001681.3:c.1420-66_1420-65insA NP_001672.1:n.1420-66_1420-65insA
NM_170665.3:c.1420-66_1420-65insA NP_733765.1:n.1420-66_1420-65insA
XM_005253888.1:c.1420-66_1420-65insA XP_005253945.1:n.1420-66_1420-65insA
XM_011538402.1:c.1420-66_1420-65insA XP_011536704.1:n.1420-66_1420-65insA
XM_011538403.1:c.1420-66_1420-65insA XP_011536705.1:n.1420-66_1420-65insA
XR_243009.1:n.1426-66_1426-65insA
XM_005253888.3:c.1420-66_1420-65insA XP_005253945.1:n.1420-66_1420-65insA
XM_011538402.3:c.1420-66_1420-65insA XP_011536704.1:n.1420-66_1420-65insA
XR_002957329.1:n.1426-66_1426-65insA
XR_243009.3:n.1426-66_1426-65insA
NM_170665.4:c.1420-66_1420-65insA MANE Select NP_733765.1:n.1420-66_1420-65insA
NM_001681.4:c.1420-66_1420-65insA NP_001672.1:n.1420-66_1420-65insA