Canonical Allele Identifier: CA481739040

Gene: ATP2A2

Linked Data

• gnomAD v4: 12-110345311-T-C
• MyVariant Identifiers: chr12:g.110783116T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345311T>C , CM000674.2:g.110345311T>C	GRCh38
NC_000012.11:g.110783116T>C , CM000674.1:g.110783116T>C	GRCh37
NC_000012.10:g.109267499T>C	NCBI36
NG_007097.2:g.68685T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2670T>C MANE Select	ENSP00000440045.2:p.Phe890=
ENST00000308664.10:c.2670T>C	ENSP00000311186.6:p.Phe890=
ENST00000377685.9:c.*2510T>C	ENSP00000366913.4:n.*2510T>C
ENST00000539276.6:c.2670T>C	ENSP00000440045.2:p.Phe890=
ENST00000548169.2:c.2341T>C
NM_001681.3:c.2670T>C	NP_001672.1:p.Phe890=
NM_170665.3:c.2670T>C	NP_733765.1:p.Phe890=
XM_005253888.1:c.2670T>C	XP_005253945.1:p.Phe890=
XM_011538402.1:c.2670T>C	XP_011536704.1:p.Phe890=
XR_243009.1:n.2676T>C
XM_005253888.3:c.2670T>C	XP_005253945.1:p.Phe890=
XM_011538402.3:c.2670T>C	XP_011536704.1:p.Phe890=
XR_002957329.1:n.2676T>C
XR_243009.3:n.2676T>C
NM_170665.4:c.2670T>C MANE Select	NP_733765.1:p.Phe890=
NM_001681.4:c.2670T>C	NP_001672.1:p.Phe890=