Canonical Allele Identifier: CA1139662869

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110281753G>C , CM000674.2:g.110281753G>C	GRCh38
NC_000012.11:g.110719558G>C , CM000674.1:g.110719558G>C	GRCh37
NC_000012.10:g.109203941G>C	NCBI36
NG_007097.2:g.5127G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_170665.4:c.-37G>C MANE Select	NP_733765.1:n.-37G>C
ENST00000539276.7:c.-37G>C MANE Select	ENSP00000440045.2:n.-37G>C
NM_001681.3:c.-37G>C	NP_001672.1:n.-37G>C
NM_001681.4:c.-37G>C	NP_001672.1:n.-37G>C
NM_170665.3:c.-37G>C	NP_733765.1:n.-37G>C
ENST00000308664.10:c.-37G>C	ENSP00000311186.6:n.-37G>C
ENST00000377685.9:c.-37G>C	ENSP00000366913.4:n.-37G>C
ENST00000539276.6:c.-37G>C	ENSP00000440045.2:n.-37G>C
ENST00000552636.1:c.-184+789G>C	ENSP00000447406.1:n.-184+789G>C
ENST00000552636.2:c.-258+789G>C	ENSP00000447406.2:n.-258+789G>C