Canonical Allele Identifier: CA2830554320

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345086_110345087insG , CM000674.2:g.110345086_110345087insG	GRCh38
NC_000012.11:g.110782891_110782892insG , CM000674.1:g.110782891_110782892insG	GRCh37
NC_000012.10:g.109267274_109267275insG	NCBI36
NG_007097.2:g.68460_68461insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2607+115_2607+116insG MANE Select	ENSP00000440045.2:n.2607+115_2607+116insG
ENST00000308664.10:c.2607+115_2607+116insG	ENSP00000311186.6:n.2607+115_2607+116insG
ENST00000377685.9:c.*2447+115_*2447+116insG	ENSP00000366913.4:n.*2447+115_*2447+116insG
ENST00000539276.6:c.2607+115_2607+116insG	ENSP00000440045.2:n.2607+115_2607+116insG
ENST00000547792.1:n.380_381insG
ENST00000548169.2:c.2278+115_2278+116insG
NM_001681.3:c.2607+115_2607+116insG	NP_001672.1:n.2607+115_2607+116insG
NM_170665.3:c.2607+115_2607+116insG	NP_733765.1:n.2607+115_2607+116insG
XM_005253888.1:c.2607+115_2607+116insG	XP_005253945.1:n.2607+115_2607+116insG
XM_011538402.1:c.2607+115_2607+116insG	XP_011536704.1:n.2607+115_2607+116insG
XR_243009.1:n.2613+115_2613+116insG
XM_005253888.3:c.2607+115_2607+116insG	XP_005253945.1:n.2607+115_2607+116insG
XM_011538402.3:c.2607+115_2607+116insG	XP_011536704.1:n.2607+115_2607+116insG
XR_002957329.1:n.2613+115_2613+116insG
XR_243009.3:n.2613+115_2613+116insG
NM_170665.4:c.2607+115_2607+116insG MANE Select	NP_733765.1:n.2607+115_2607+116insG
NM_001681.4:c.2607+115_2607+116insG	NP_001672.1:n.2607+115_2607+116insG