Canonical Allele Identifier: CA343951939

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925336A>T (hg19) ; chr1:g.186956204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956204A>T , CM000663.2:g.186956204A>T	GRCh38
NC_000001.10:g.186925336A>T , CM000663.1:g.186925336A>T	GRCh37
NC_000001.9:g.185191959A>T	NCBI36
NG_012203.1:g.132305A>T
NG_012203.2:g.132305A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1439A>T MANE Select	ENSP00000356436.3:p.Asn480Ile
ENST00000367466.3:c.1439A>T	ENSP00000356436.3:p.Asn480Ile
NM_001311193.1:c.1259A>T	NP_001298122.1:p.Asn420Ile
NM_024420.2:c.1439A>T	NP_077734.1:p.Asn480Ile
XM_005245267.2:c.1328A>T	XP_005245324.1:p.Asn443Ile
XM_011509641.1:c.1460A>T	XP_011507943.1:p.Asn487Ile
XM_011509642.1:c.1439A>T	XP_011507944.1:p.Asn480Ile
XM_011509643.1:c.1439A>T	XP_011507945.1:p.Asn480Ile
XR_921838.1:n.1477+23A>T
XM_005245267.4:c.1454A>T	XP_005245324.2:p.Asn485Ile
XM_011509642.2:c.1439A>T	XP_011507944.1:p.Asn480Ile
NM_001311193.2:c.1259A>T	NP_001298122.2:p.Asn420Ile
NM_024420.3:c.1439A>T MANE Select	NP_077734.2:p.Asn480Ile