Canonical Allele Identifier: CA395415521

Gene: ATP2A1

Linked Data

• dbSNP Id: rs1410348656
• gnomAD v2: 16-28914409-G-C
• gnomAD v4: 16-28903088-G-C
• MyVariant Identifiers: chr16:g.28914409G>C (hg19) ; chr16:g.28903088G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28903088G>C , CM000678.2:g.28903088G>C	GRCh38
NC_000016.9:g.28914409G>C , CM000678.1:g.28914409G>C	GRCh37
NC_000016.8:g.28821910G>C	NCBI36
NG_023327.1:g.29601G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395503.9:c.2803G>C MANE Select	ENSP00000378879.5:p.Gly935Arg
ENST00000357084.7:c.2803G>C	ENSP00000349595.3:p.Gly935Arg
ENST00000395503.8:c.2803G>C	ENSP00000378879.4:p.Gly935Arg
ENST00000536376.5:c.2428G>C	ENSP00000443101.1:p.Gly810Arg
NM_001286075.1:c.2428G>C	NP_001273004.1:p.Gly810Arg
NM_004320.4:c.2803G>C	NP_004311.1:p.Gly935Arg
NM_173201.3:c.2803G>C	NP_775293.1:p.Gly935Arg
NM_004320.6:c.2803G>C MANE Select	NP_004311.1:p.Gly935Arg
NM_173201.4:c.2803G>C	NP_775293.1:p.Gly935Arg
NM_001286075.2:c.2428G>C	NP_001273004.1:p.Gly810Arg
NM_173201.5:c.2803G>C	NP_775293.1:p.Gly935Arg