Canonical Allele Identifier: CA339253783
Gene: PLA2G2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19978434T>C , CM000663.2:g.19978434T>C GRCh38
NC_000001.10:g.20304927T>C , CM000663.1:g.20304927T>C GRCh37
NC_000001.9:g.20177514T>C NCBI36
NG_012928.1:g.7006A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000482011.3:c.131A>G MANE Select ENSP00000504762.1:p.Tyr44Cys
ENST00000400520.8:c.131A>G ENSP00000383364.3:p.Tyr44Cys
ENST00000482011.2:c.131A>G ENSP00000504762.1:p.Tyr44Cys
ENST00000649436.1:c.50A>G ENSP00000496912.1:p.Tyr17Cys
ENST00000375111.7:c.131A>G ENSP00000364252.3:p.Tyr44Cys
ENST00000400520.7:c.131A>G ENSP00000383364.3:p.Tyr44Cys
ENST00000461140.1:n.385A>G
ENST00000469162.5:n.297A>G
ENST00000482011.1:n.403A>G
ENST00000491964.5:n.363A>G
ENST00000496748.1:n.481A>G
NM_000300.3:c.131A>G NP_000291.1:p.Tyr44Cys
NM_001161727.1:c.131A>G NP_001155199.1:p.Tyr44Cys
NM_001161728.1:c.131A>G NP_001155200.1:p.Tyr44Cys
NM_001161729.1:c.131A>G NP_001155201.1:p.Tyr44Cys
NM_000300.4:c.131A>G NP_000291.1:p.Tyr44Cys
NM_001161727.2:c.131A>G NP_001155199.1:p.Tyr44Cys
NM_001161728.2:c.131A>G NP_001155200.1:p.Tyr44Cys
NM_001395463.1:c.131A>G MANE Select NP_001382392.1:p.Tyr44Cys