Canonical Allele Identifier: CA343951814
Gene: PLA2G4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186956192C>T , CM000663.2:g.186956192C>T GRCh38
NC_000001.10:g.186925324C>T , CM000663.1:g.186925324C>T GRCh37
NC_000001.9:g.185191947C>T NCBI36
NG_012203.1:g.132293C>T
NG_012203.2:g.132293C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.1427C>T MANE Select ENSP00000356436.3:p.Ser476Leu
ENST00000367466.3:c.1427C>T ENSP00000356436.3:p.Ser476Leu
NM_001311193.1:c.1247C>T NP_001298122.1:p.Ser416Leu
NM_024420.2:c.1427C>T NP_077734.1:p.Ser476Leu
XM_005245267.2:c.1316C>T XP_005245324.1:p.Ser439Leu
XM_011509641.1:c.1448C>T XP_011507943.1:p.Ser483Leu
XM_011509642.1:c.1427C>T XP_011507944.1:p.Ser476Leu
XM_011509643.1:c.1427C>T XP_011507945.1:p.Ser476Leu
XR_921838.1:n.1477+11C>T
XM_005245267.4:c.1442C>T XP_005245324.2:p.Ser481Leu
XM_011509642.2:c.1427C>T XP_011507944.1:p.Ser476Leu
NM_001311193.2:c.1247C>T NP_001298122.2:p.Ser416Leu
NM_024420.3:c.1427C>T MANE Select NP_077734.2:p.Ser476Leu