Canonical Allele Identifier: CA14341022

Gene: ATP2C2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84389428G>A , CM000678.2:g.84389428G>A	GRCh38
NC_000016.9:g.84423034G>A , CM000678.1:g.84423034G>A	GRCh37
NC_000016.8:g.82980535G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262429.9:c.100-9071G>A MANE Select	ENSP00000262429.4:n.100-9071G>A
ENST00000262429.8:c.100-9071G>A	ENSP00000262429.4:n.100-9071G>A
ENST00000416219.6:c.100-9071G>A	ENSP00000397925.2:n.100-9071G>A
NM_001286527.2:c.100-9071G>A	NP_001273456.2:n.100-9071G>A
NM_014861.3:c.100-9071G>A	NP_055676.3:n.100-9071G>A
XR_001752045.1:n.193-9071G>A
NM_001286527.3:c.100-9071G>A	NP_001273456.2:n.100-9071G>A
NM_014861.4:c.100-9071G>A MANE Select	NP_055676.3:n.100-9071G>A