Canonical Allele Identifier: CA2732573935

Gene: ATP2C2

Linked Data

• dbSNP Id: rs201435809

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84412781dup , CM000678.2:g.84412781dup	GRCh38
NC_000016.9:g.84446387dup , CM000678.1:g.84446387dup	GRCh37
NC_000016.8:g.83003888dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262429.9:c.515+2016dup MANE Select	ENSP00000262429.4:n.515+2016dup
ENST00000262429.8:c.515+2016dup	ENSP00000262429.4:n.515+2016dup
ENST00000416219.6:c.515+2016dup	ENSP00000397925.2:n.515+2016dup
ENST00000420010.6:n.188+2178dup
ENST00000565546.5:n.250+2016dup
ENST00000565631.5:n.1006+2016dup
ENST00000565927.1:n.504+2016dup
ENST00000569207.5:c.237+2016dup
NM_001286527.2:c.515+2016dup	NP_001273456.2:n.515+2016dup
NM_001291454.1:c.62+2178dup	NP_001278383.1:n.62+2178dup
NM_014861.3:c.515+2016dup	NP_055676.3:n.515+2016dup
XM_011523486.1:c.446+2016dup	XP_011521788.1:n.446+2016dup
XM_011523486.2:c.446+2016dup	XP_011521788.1:n.446+2016dup
XR_001752045.1:n.608+2016dup
NM_001286527.3:c.515+2016dup	NP_001273456.2:n.515+2016dup
NM_001291454.2:c.62+2178dup	NP_001278383.1:n.62+2178dup
NM_014861.4:c.515+2016dup MANE Select	NP_055676.3:n.515+2016dup