Canonical Allele Identifier: CA343952373

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925388T>G (hg19) ; chr1:g.186956256T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956256T>G , CM000663.2:g.186956256T>G	GRCh38
NC_000001.10:g.186925388T>G , CM000663.1:g.186925388T>G	GRCh37
NC_000001.9:g.185192011T>G	NCBI36
NG_012203.1:g.132357T>G
NG_012203.2:g.132357T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1491T>G MANE Select	ENSP00000356436.3:p.Asn497Lys
ENST00000367466.3:c.1491T>G	ENSP00000356436.3:p.Asn497Lys
NM_001311193.1:c.1311T>G	NP_001298122.1:p.Asn437Lys
NM_024420.2:c.1491T>G	NP_077734.1:p.Asn497Lys
XM_005245267.2:c.1380T>G	XP_005245324.1:p.Asn460Lys
XM_011509641.1:c.1512T>G	XP_011507943.1:p.Asn504Lys
XM_011509642.1:c.1491T>G	XP_011507944.1:p.Asn497Lys
XM_011509643.1:c.1491T>G	XP_011507945.1:p.Asn497Lys
XR_921838.1:n.1477+75T>G
XM_005245267.4:c.1506T>G	XP_005245324.2:p.Asn502Lys
XM_011509642.2:c.1491T>G	XP_011507944.1:p.Asn497Lys
NM_001311193.2:c.1311T>G	NP_001298122.2:p.Asn437Lys
NM_024420.3:c.1491T>G MANE Select	NP_077734.2:p.Asn497Lys