Canonical Allele Identifier: CA2062803850

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110339886_110339887delinsCA , CM000674.2:g.110339886_110339887delinsCA	GRCh38
NC_000012.11:g.110777691_110777692delinsCA , CM000674.1:g.110777691_110777692delinsCA	GRCh37
NC_000012.10:g.109262074_109262075delinsCA	NCBI36
NG_007097.2:g.63260_63261delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.1761+165_1761+166delinsCA MANE Select	ENSP00000440045.2:n.1761+165_1761+166delinsCA
ENST00000308664.10:c.1761+165_1761+166delinsCA	ENSP00000311186.6:n.1761+165_1761+166delinsCA
ENST00000377685.9:c.*1601+165_*1601+166delinsCA	ENSP00000366913.4:n.*1601+165_*1601+166delinsCA
ENST00000539276.6:c.1761+165_1761+166delinsCA	ENSP00000440045.2:n.1761+165_1761+166delinsCA
ENST00000548169.2:c.1432+165_1432+166delinsCA
NM_001681.3:c.1761+165_1761+166delinsCA	NP_001672.1:n.1761+165_1761+166delinsCA
NM_170665.3:c.1761+165_1761+166delinsCA	NP_733765.1:n.1761+165_1761+166delinsCA
XM_005253888.1:c.1761+165_1761+166delinsCA	XP_005253945.1:n.1761+165_1761+166delinsCA
XM_011538402.1:c.1761+165_1761+166delinsCA	XP_011536704.1:n.1761+165_1761+166delinsCA
XM_011538403.1:c.1761+165_1761+166delinsCA	XP_011536705.1:n.1761+165_1761+166delinsCA
XR_243009.1:n.1767+165_1767+166delinsCA
XM_005253888.3:c.1761+165_1761+166delinsCA	XP_005253945.1:n.1761+165_1761+166delinsCA
XM_011538402.3:c.1761+165_1761+166delinsCA	XP_011536704.1:n.1761+165_1761+166delinsCA
XR_002957329.1:n.1767+165_1767+166delinsCA
XR_243009.3:n.1767+165_1767+166delinsCA
NM_170665.4:c.1761+165_1761+166delinsCA MANE Select	NP_733765.1:n.1761+165_1761+166delinsCA
NM_001681.4:c.1761+165_1761+166delinsCA	NP_001672.1:n.1761+165_1761+166delinsCA