Canonical Allele Identifier: CA343952142

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925365C>G (hg19) ; chr1:g.186956233C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956233C>G , CM000663.2:g.186956233C>G	GRCh38
NC_000001.10:g.186925365C>G , CM000663.1:g.186925365C>G	GRCh37
NC_000001.9:g.185191988C>G	NCBI36
NG_012203.1:g.132334C>G
NG_012203.2:g.132334C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1468C>G MANE Select	ENSP00000356436.3:p.His490Asp
ENST00000367466.3:c.1468C>G	ENSP00000356436.3:p.His490Asp
NM_001311193.1:c.1288C>G	NP_001298122.1:p.His430Asp
NM_024420.2:c.1468C>G	NP_077734.1:p.His490Asp
XM_005245267.2:c.1357C>G	XP_005245324.1:p.His453Asp
XM_011509641.1:c.1489C>G	XP_011507943.1:p.His497Asp
XM_011509642.1:c.1468C>G	XP_011507944.1:p.His490Asp
XM_011509643.1:c.1468C>G	XP_011507945.1:p.His490Asp
XR_921838.1:n.1477+52C>G
XM_005245267.4:c.1483C>G	XP_005245324.2:p.His495Asp
XM_011509642.2:c.1468C>G	XP_011507944.1:p.His490Asp
NM_001311193.2:c.1288C>G	NP_001298122.2:p.His430Asp
NM_024420.3:c.1468C>G MANE Select	NP_077734.2:p.His490Asp