Canonical Allele Identifier: CA343951865

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925330T>C (hg19) ; chr1:g.186956198T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956198T>C , CM000663.2:g.186956198T>C	GRCh38
NC_000001.10:g.186925330T>C , CM000663.1:g.186925330T>C	GRCh37
NC_000001.9:g.185191953T>C	NCBI36
NG_012203.1:g.132299T>C
NG_012203.2:g.132299T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1433T>C MANE Select	ENSP00000356436.3:p.Leu478Ser
ENST00000367466.3:c.1433T>C	ENSP00000356436.3:p.Leu478Ser
NM_001311193.1:c.1253T>C	NP_001298122.1:p.Leu418Ser
NM_024420.2:c.1433T>C	NP_077734.1:p.Leu478Ser
XM_005245267.2:c.1322T>C	XP_005245324.1:p.Leu441Ser
XM_011509641.1:c.1454T>C	XP_011507943.1:p.Leu485Ser
XM_011509642.1:c.1433T>C	XP_011507944.1:p.Leu478Ser
XM_011509643.1:c.1433T>C	XP_011507945.1:p.Leu478Ser
XR_921838.1:n.1477+17T>C
XM_005245267.4:c.1448T>C	XP_005245324.2:p.Leu483Ser
XM_011509642.2:c.1433T>C	XP_011507944.1:p.Leu478Ser
NM_001311193.2:c.1253T>C	NP_001298122.2:p.Leu418Ser
NM_024420.3:c.1433T>C MANE Select	NP_077734.2:p.Leu478Ser