Canonical Allele Identifier: CA1157333898

Gene: PLA2G2A

Linked Data

• dbSNP Id: rs2046255365

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978445del , CM000663.2:g.19978445del	GRCh38
NC_000001.10:g.20304938del , CM000663.1:g.20304938del	GRCh37
NC_000001.9:g.20177525del	NCBI36
NG_012928.1:g.6996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482011.3:c.121del MANE Select	ENSP00000504762.1:p.Tyr41MetfsTer?
ENST00000400520.8:c.121del	ENSP00000383364.3:p.Tyr41MetfsTer?
ENST00000482011.2:c.121del	ENSP00000504762.1:p.Tyr41MetfsTer?
ENST00000649436.1:c.40del	ENSP00000496912.1:p.Tyr14MetfsTer?
ENST00000375111.7:c.121del	ENSP00000364252.3:p.Tyr41MetfsTer?
ENST00000400520.7:c.121del	ENSP00000383364.3:p.Tyr41MetfsTer?
ENST00000461140.1:n.375del
ENST00000469162.5:n.287del
ENST00000482011.1:n.393del
ENST00000491964.5:n.353del
ENST00000496748.1:n.471del
NM_000300.3:c.121del	NP_000291.1:p.Tyr41MetfsTer?
NM_001161727.1:c.121del	NP_001155199.1:p.Tyr41MetfsTer?
NM_001161728.1:c.121del	NP_001155200.1:p.Tyr41MetfsTer?
NM_001161729.1:c.121del	NP_001155201.1:p.Tyr41MetfsTer?
NM_000300.4:c.121del	NP_000291.1:p.Tyr41MetfsTer?
NM_001161727.2:c.121del	NP_001155199.1:p.Tyr41MetfsTer?
NM_001161728.2:c.121del	NP_001155200.1:p.Tyr41MetfsTer?
NM_001395463.1:c.121del MANE Select	NP_001382392.1:p.Tyr41MetfsTer?