Canonical Allele Identifier: CA416639632

Gene: PLA2G2A

Linked Data

• MyVariant Identifiers: chr1:g.20304989C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978496C>G , CM000663.2:g.19978496C>G	GRCh38
NC_000001.10:g.20304989C>G , CM000663.1:g.20304989C>G	GRCh37
NC_000001.9:g.20177576C>G	NCBI36
NG_012928.1:g.6944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.69G>C MANE Select	ENSP00000504762.1:p.Val23=
ENST00000400520.8:c.69G>C	ENSP00000383364.3:p.Val23=
ENST00000482011.2:c.69G>C	ENSP00000504762.1:p.Val23=
ENST00000649436.1:c.-1-12G>C	ENSP00000496912.1:n.-1-12G>C
ENST00000375111.7:c.69G>C	ENSP00000364252.3:p.Val23=
ENST00000400520.7:c.69G>C	ENSP00000383364.3:p.Val23=
ENST00000461140.1:n.335-12G>C
ENST00000469162.5:n.235G>C
ENST00000482011.1:n.341G>C
ENST00000491964.5:n.301G>C
ENST00000496748.1:n.419G>C
NM_000300.3:c.69G>C	NP_000291.1:p.Val23=
NM_001161727.1:c.69G>C	NP_001155199.1:p.Val23=
NM_001161728.1:c.69G>C	NP_001155200.1:p.Val23=
NM_001161729.1:c.69G>C	NP_001155201.1:p.Val23=
NM_000300.4:c.69G>C	NP_000291.1:p.Val23=
NM_001161727.2:c.69G>C	NP_001155199.1:p.Val23=
NM_001161728.2:c.69G>C	NP_001155200.1:p.Val23=
NM_001395463.1:c.69G>C MANE Select	NP_001382392.1:p.Val23=