Canonical Allele Identifier: CA339253759

Gene: PLA2G2A

Linked Data

• MyVariant Identifiers: chr1:g.20304916A>T (hg19) ; chr1:g.19978423A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978423A>T , CM000663.2:g.19978423A>T	GRCh38
NC_000001.10:g.20304916A>T , CM000663.1:g.20304916A>T	GRCh37
NC_000001.9:g.20177503A>T	NCBI36
NG_012928.1:g.7017T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.142T>A MANE Select	ENSP00000504762.1:p.Cys48Ser
ENST00000400520.8:c.142T>A	ENSP00000383364.3:p.Cys48Ser
ENST00000482011.2:c.142T>A	ENSP00000504762.1:p.Cys48Ser
ENST00000649436.1:c.61T>A	ENSP00000496912.1:p.Cys21Ser
ENST00000375111.7:c.142T>A	ENSP00000364252.3:p.Cys48Ser
ENST00000400520.7:c.142T>A	ENSP00000383364.3:p.Cys48Ser
ENST00000461140.1:n.396T>A
ENST00000469162.5:n.308T>A
ENST00000482011.1:n.414T>A
ENST00000491964.5:n.374T>A
ENST00000496748.1:n.492T>A
NM_000300.3:c.142T>A	NP_000291.1:p.Cys48Ser
NM_001161727.1:c.142T>A	NP_001155199.1:p.Cys48Ser
NM_001161728.1:c.142T>A	NP_001155200.1:p.Cys48Ser
NM_001161729.1:c.142T>A	NP_001155201.1:p.Cys48Ser
NM_000300.4:c.142T>A	NP_000291.1:p.Cys48Ser
NM_001161727.2:c.142T>A	NP_001155199.1:p.Cys48Ser
NM_001161728.2:c.142T>A	NP_001155200.1:p.Cys48Ser
NM_001395463.1:c.142T>A MANE Select	NP_001382392.1:p.Cys48Ser