Canonical Allele Identifier: CA623866029

Gene: ATP2C2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84412778C>A , CM000678.2:g.84412778C>A	GRCh38
NC_000016.9:g.84446384C>A , CM000678.1:g.84446384C>A	GRCh37
NC_000016.8:g.83003885C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262429.9:c.515+2013C>A MANE Select	ENSP00000262429.4:n.515+2013C>A
ENST00000262429.8:c.515+2013C>A	ENSP00000262429.4:n.515+2013C>A
ENST00000416219.6:c.515+2013C>A	ENSP00000397925.2:n.515+2013C>A
ENST00000420010.6:n.188+2175C>A
ENST00000565546.5:n.250+2013C>A
ENST00000565631.5:n.1006+2013C>A
ENST00000565927.1:n.504+2013C>A
ENST00000569207.5:c.237+2013C>A
NM_001286527.2:c.515+2013C>A	NP_001273456.2:n.515+2013C>A
NM_001291454.1:c.62+2175C>A	NP_001278383.1:n.62+2175C>A
NM_014861.3:c.515+2013C>A	NP_055676.3:n.515+2013C>A
XM_011523486.1:c.446+2013C>A	XP_011521788.1:n.446+2013C>A
XM_011523486.2:c.446+2013C>A	XP_011521788.1:n.446+2013C>A
XR_001752045.1:n.608+2013C>A
NM_001286527.3:c.515+2013C>A	NP_001273456.2:n.515+2013C>A
NM_001291454.2:c.62+2175C>A	NP_001278383.1:n.62+2175C>A
NM_014861.4:c.515+2013C>A MANE Select	NP_055676.3:n.515+2013C>A