Canonical Allele Identifier: CA494874305

Gene: ATP2A1

Linked Data

• MyVariant Identifiers: chr16:g.28911943T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28900622T>C , CM000678.2:g.28900622T>C	GRCh38
NC_000016.9:g.28911943T>C , CM000678.1:g.28911943T>C	GRCh37
NC_000016.8:g.28819444T>C	NCBI36
NG_023327.1:g.27135T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395503.9:c.1806T>C MANE Select	ENSP00000378879.5:p.Pro602=
ENST00000357084.7:c.1806T>C	ENSP00000349595.3:p.Pro602=
ENST00000395503.8:c.1806T>C	ENSP00000378879.4:p.Pro602=
ENST00000536376.5:c.1431T>C	ENSP00000443101.1:p.Pro477=
NM_001286075.1:c.1431T>C	NP_001273004.1:p.Pro477=
NM_004320.4:c.1806T>C	NP_004311.1:p.Pro602=
NM_173201.3:c.1806T>C	NP_775293.1:p.Pro602=
NM_004320.6:c.1806T>C MANE Select	NP_004311.1:p.Pro602=
NM_173201.4:c.1806T>C	NP_775293.1:p.Pro602=
NM_001286075.2:c.1431T>C	NP_001273004.1:p.Pro477=
NM_173201.5:c.1806T>C	NP_775293.1:p.Pro602=