Canonical Allele Identifier: CA119151

Gene: PLA2G7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.46705206A>G , CM000668.2:g.46705206A>G	GRCh38
NC_000006.11:g.46672943A>G , CM000668.1:g.46672943A>G	GRCh37
NC_000006.10:g.46780902A>G	NCBI36
NG_016204.1:g.35488T>C
NG_051941.1:g.29939A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274793.12:c.1136T>C MANE Select	ENSP00000274793.7:p.Val379Ala
ENST00000274793.11:c.1136T>C	ENSP00000274793.7:p.Val379Ala
ENST00000537365.1:c.1136T>C	ENSP00000445666.1:p.Val379Ala
NM_001168357.1:c.1136T>C	NP_001161829.1:p.Val379Ala
NM_005084.3:c.1136T>C	NP_005075.3:p.Val379Ala
XM_005249408.3:c.1136T>C	XP_005249465.1:p.Val379Ala
XM_005249408.4:c.1136T>C	XP_005249465.1:p.Val379Ala
XR_001743639.2:n.1290T>C
XR_002956305.1:n.3472T>C
NM_005084.4:c.1136T>C MANE Select	NP_005075.3:p.Val379Ala
NM_001168357.2:c.1136T>C	NP_001161829.1:p.Val379Ala