Canonical Allele Identifier: CA343951717

Gene: PLA2G4A

Linked Data

• MyVariant Identifiers: chr1:g.186925312T>A (hg19) ; chr1:g.186956180T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186956180T>A , CM000663.2:g.186956180T>A	GRCh38
NC_000001.10:g.186925312T>A , CM000663.1:g.186925312T>A	GRCh37
NC_000001.9:g.185191935T>A	NCBI36
NG_012203.1:g.132281T>A
NG_012203.2:g.132281T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367466.4:c.1415T>A MANE Select	ENSP00000356436.3:p.Leu472Ter
ENST00000367466.3:c.1415T>A	ENSP00000356436.3:p.Leu472Ter
NM_001311193.1:c.1235T>A	NP_001298122.1:p.Leu412Ter
NM_024420.2:c.1415T>A	NP_077734.1:p.Leu472Ter
XM_005245267.2:c.1304T>A	XP_005245324.1:p.Leu435Ter
XM_011509641.1:c.1436T>A	XP_011507943.1:p.Leu479Ter
XM_011509642.1:c.1415T>A	XP_011507944.1:p.Leu472Ter
XM_011509643.1:c.1415T>A	XP_011507945.1:p.Leu472Ter
XR_921838.1:n.1476T>A
XM_005245267.4:c.1430T>A	XP_005245324.2:p.Leu477Ter
XM_011509642.2:c.1415T>A	XP_011507944.1:p.Leu472Ter
NM_001311193.2:c.1235T>A	NP_001298122.2:p.Leu412Ter
NM_024420.3:c.1415T>A MANE Select	NP_077734.2:p.Leu472Ter