Canonical Allele Identifier: CA344312309

Gene: ATP2B4

Linked Data

• MyVariant Identifiers: chr1:g.203672841C>G (hg19) ; chr1:g.203703713C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203703713C>G , CM000663.2:g.203703713C>G	GRCh38
NC_000001.10:g.203672841C>G , CM000663.1:g.203672841C>G	GRCh37
NC_000001.9:g.201939464C>G	NCBI36
NG_029589.1:g.81927C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341360.7:c.999C>G	ENSP00000340930.2:p.Asp333Glu
ENST00000705901.1:c.963C>G	ENSP00000516177.1:p.Asp321Glu
ENST00000357681.10:c.999C>G MANE Select	ENSP00000350310.5:p.Asp333Glu
ENST00000341360.6:c.999C>G	ENSP00000340930.2:p.Asp333Glu
ENST00000357681.9:c.999C>G	ENSP00000350310.5:p.Asp333Glu
ENST00000367218.7:c.999C>G	ENSP00000356187.3:p.Asp333Glu
NM_001001396.2:c.999C>G	NP_001001396.1:p.Asp333Glu
NM_001684.4:c.999C>G	NP_001675.3:p.Asp333Glu
NM_001365783.1:c.999C>G	NP_001352712.1:p.Asp333Glu
NM_001365784.1:c.999C>G	NP_001352713.1:p.Asp333Glu
NM_001365783.2:c.999C>G	NP_001352712.1:p.Asp333Glu
NM_001684.5:c.999C>G MANE Select	NP_001675.3:p.Asp333Glu
NM_001001396.3:c.999C>G	NP_001001396.1:p.Asp333Glu
NM_001365784.2:c.999C>G	NP_001352713.1:p.Asp333Glu