Canonical Allele Identifier: CA2830554319

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345085_110345086insTG , CM000674.2:g.110345085_110345086insTG	GRCh38
NC_000012.11:g.110782890_110782891insTG , CM000674.1:g.110782890_110782891insTG	GRCh37
NC_000012.10:g.109267273_109267274insTG	NCBI36
NG_007097.2:g.68459_68460insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2607+114_2607+115insTG MANE Select	ENSP00000440045.2:n.2607+114_2607+115insTG
ENST00000308664.10:c.2607+114_2607+115insTG	ENSP00000311186.6:n.2607+114_2607+115insTG
ENST00000377685.9:c.*2447+114_*2447+115insTG	ENSP00000366913.4:n.*2447+114_*2447+115insTG
ENST00000539276.6:c.2607+114_2607+115insTG	ENSP00000440045.2:n.2607+114_2607+115insTG
ENST00000547792.1:n.379_380insTG
ENST00000548169.2:c.2278+114_2278+115insTG
NM_001681.3:c.2607+114_2607+115insTG	NP_001672.1:n.2607+114_2607+115insTG
NM_170665.3:c.2607+114_2607+115insTG	NP_733765.1:n.2607+114_2607+115insTG
XM_005253888.1:c.2607+114_2607+115insTG	XP_005253945.1:n.2607+114_2607+115insTG
XM_011538402.1:c.2607+114_2607+115insTG	XP_011536704.1:n.2607+114_2607+115insTG
XR_243009.1:n.2613+114_2613+115insTG
XM_005253888.3:c.2607+114_2607+115insTG	XP_005253945.1:n.2607+114_2607+115insTG
XM_011538402.3:c.2607+114_2607+115insTG	XP_011536704.1:n.2607+114_2607+115insTG
XR_002957329.1:n.2613+114_2613+115insTG
XR_243009.3:n.2613+114_2613+115insTG
NM_170665.4:c.2607+114_2607+115insTG MANE Select	NP_733765.1:n.2607+114_2607+115insTG
NM_001681.4:c.2607+114_2607+115insTG	NP_001672.1:n.2607+114_2607+115insTG