Canonical Allele Identifier: CA279244675

Gene: ATP2A1

Linked Data

• dbSNP Id: rs373585900
• gnomAD v3: 16-28902978-G-A
• gnomAD v4: 16-28902978-G-A
• MyVariant Identifiers: chr16:g.28914299G>A (hg19) ; chr16:g.28902978G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28902978G>A , CM000678.2:g.28902978G>A	GRCh38
NC_000016.9:g.28914299G>A , CM000678.1:g.28914299G>A	GRCh37
NC_000016.8:g.28821800G>A	NCBI36
NG_023327.1:g.29491G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395503.9:c.2745-52G>A MANE Select	ENSP00000378879.5:n.2745-52G>A
ENST00000357084.7:c.2745-52G>A	ENSP00000349595.3:n.2745-52G>A
ENST00000395503.8:c.2745-52G>A	ENSP00000378879.4:n.2745-52G>A
ENST00000536376.5:c.2370-52G>A	ENSP00000443101.1:n.2370-52G>A
NM_001286075.1:c.2370-52G>A	NP_001273004.1:n.2370-52G>A
NM_004320.4:c.2745-52G>A	NP_004311.1:n.2745-52G>A
NM_173201.3:c.2745-52G>A	NP_775293.1:n.2745-52G>A
NM_004320.6:c.2745-52G>A MANE Select	NP_004311.1:n.2745-52G>A
NM_173201.4:c.2745-52G>A	NP_775293.1:n.2745-52G>A
NM_001286075.2:c.2370-52G>A	NP_001273004.1:n.2370-52G>A
NM_173201.5:c.2745-52G>A	NP_775293.1:n.2745-52G>A