Canonical Allele Identifier: CA339253765

Gene: PLA2G2A

Linked Data

• MyVariant Identifiers: chr1:g.20304919G>A (hg19) ; chr1:g.19978426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19978426G>A , CM000663.2:g.19978426G>A	GRCh38
NC_000001.10:g.20304919G>A , CM000663.1:g.20304919G>A	GRCh37
NC_000001.9:g.20177506G>A	NCBI36
NG_012928.1:g.7014C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000482011.3:c.139C>T MANE Select	ENSP00000504762.1:p.His47Tyr
ENST00000400520.8:c.139C>T	ENSP00000383364.3:p.His47Tyr
ENST00000482011.2:c.139C>T	ENSP00000504762.1:p.His47Tyr
ENST00000649436.1:c.58C>T	ENSP00000496912.1:p.His20Tyr
ENST00000375111.7:c.139C>T	ENSP00000364252.3:p.His47Tyr
ENST00000400520.7:c.139C>T	ENSP00000383364.3:p.His47Tyr
ENST00000461140.1:n.393C>T
ENST00000469162.5:n.305C>T
ENST00000482011.1:n.411C>T
ENST00000491964.5:n.371C>T
ENST00000496748.1:n.489C>T
NM_000300.3:c.139C>T	NP_000291.1:p.His47Tyr
NM_001161727.1:c.139C>T	NP_001155199.1:p.His47Tyr
NM_001161728.1:c.139C>T	NP_001155200.1:p.His47Tyr
NM_001161729.1:c.139C>T	NP_001155201.1:p.His47Tyr
NM_000300.4:c.139C>T	NP_000291.1:p.His47Tyr
NM_001161727.2:c.139C>T	NP_001155199.1:p.His47Tyr
NM_001161728.2:c.139C>T	NP_001155200.1:p.His47Tyr
NM_001395463.1:c.139C>T MANE Select	NP_001382392.1:p.His47Tyr