Canonical Allele Identifier: CA1626051257

Gene: PLA2G7

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.46714342A>T , CM000668.2:g.46714342A>T	GRCh38
NC_000006.11:g.46682079A>T , CM000668.1:g.46682079A>T	GRCh37
NC_000006.10:g.46790038A>T	NCBI36
NG_016204.1:g.26352T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274793.12:c.470+118T>A MANE Select	ENSP00000274793.7:n.470+118T>A
ENST00000274793.11:c.470+118T>A	ENSP00000274793.7:n.470+118T>A
ENST00000537365.1:c.470+118T>A	ENSP00000445666.1:n.470+118T>A
NM_001168357.1:c.470+118T>A	NP_001161829.1:n.470+118T>A
NM_005084.3:c.470+118T>A	NP_005075.3:n.470+118T>A
XM_005249408.3:c.470+118T>A	XP_005249465.1:n.470+118T>A
XM_005249409.2:c.470+118T>A	XP_005249466.1:n.470+118T>A
XM_005249408.4:c.470+118T>A	XP_005249465.1:n.470+118T>A
XR_001743639.2:n.716+118T>A
XR_002956305.1:n.515+118T>A
NM_005084.4:c.470+118T>A MANE Select	NP_005075.3:n.470+118T>A
NM_001168357.2:c.470+118T>A	NP_001161829.1:n.470+118T>A