Canonical Allele Identifier: CA658039

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs142941380
• ExAC: 1:20304910 C / T
• gnomAD v2: 1-20304910-C-T
• gnomAD v3: 1-19978417-C-T
• gnomAD v4: 1-19978417-C-T
• COSMIC: COSM3481807
• MyVariant Identifiers: chr1:g.20304910C>T (hg19) ; chr1:g.19978417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978417C>T , CM000663.2:g.19978417C>T	GRCh38
NC_000001.10:g.20304910C>T , CM000663.1:g.20304910C>T	GRCh37
NC_000001.9:g.20177497C>T	NCBI36
NG_012928.1:g.7023G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.148G>A MANE Select	ENSP00000504762.1:p.Val50Met
ENST00000400520.8:c.148G>A	ENSP00000383364.3:p.Val50Met
ENST00000482011.2:c.148G>A	ENSP00000504762.1:p.Val50Met
ENST00000649436.1:c.67G>A	ENSP00000496912.1:p.Val23Met
ENST00000375111.7:c.148G>A	ENSP00000364252.3:p.Val50Met
ENST00000400520.7:c.148G>A	ENSP00000383364.3:p.Val50Met
ENST00000461140.1:n.402G>A
ENST00000469162.5:n.314G>A
ENST00000482011.1:n.420G>A
ENST00000491964.5:n.380G>A
ENST00000496748.1:n.498G>A
NM_000300.3:c.148G>A	NP_000291.1:p.Val50Met
NM_001161727.1:c.148G>A	NP_001155199.1:p.Val50Met
NM_001161728.1:c.148G>A	NP_001155200.1:p.Val50Met
NM_001161729.1:c.148G>A	NP_001155201.1:p.Val50Met
NM_000300.4:c.148G>A	NP_000291.1:p.Val50Met
NM_001161727.2:c.148G>A	NP_001155199.1:p.Val50Met
NM_001161728.2:c.148G>A	NP_001155200.1:p.Val50Met
NM_001395463.1:c.148G>A MANE Select	NP_001382392.1:p.Val50Met