Canonical Allele Identifier: CA343951443

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925276A>C (hg19) ; chr1:g.186956144A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956144A>C , CM000663.2:g.186956144A>C	GRCh38
NC_000001.10:g.186925276A>C , CM000663.1:g.186925276A>C	GRCh37
NC_000001.9:g.185191899A>C	NCBI36
NG_012203.1:g.132245A>C
NG_012203.2:g.132245A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1379A>C MANE Select	ENSP00000356436.3:p.Asn460Thr
ENST00000367466.3:c.1379A>C	ENSP00000356436.3:p.Asn460Thr
NM_001311193.1:c.1199A>C	NP_001298122.1:p.Asn400Thr
NM_024420.2:c.1379A>C	NP_077734.1:p.Asn460Thr
XM_005245267.2:c.1268A>C	XP_005245324.1:p.Asn423Thr
XM_011509641.1:c.1400A>C	XP_011507943.1:p.Asn467Thr
XM_011509642.1:c.1379A>C	XP_011507944.1:p.Asn460Thr
XM_011509643.1:c.1379A>C	XP_011507945.1:p.Asn460Thr
XR_921838.1:n.1440A>C
XM_005245267.4:c.1394A>C	XP_005245324.2:p.Asn465Thr
XM_011509642.2:c.1379A>C	XP_011507944.1:p.Asn460Thr
NM_001311193.2:c.1199A>C	NP_001298122.2:p.Asn400Thr
NM_024420.3:c.1379A>C MANE Select	NP_077734.2:p.Asn460Thr