Canonical Allele Identifier: CA1626042313
Community Standard Title: NM_005084.4(PLA2G7):c.1136T= (p.Val379=)
Gene: PLA2G7 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_005084.4:c.1136T= MANE Select NP_005075.3:p.Val379=
ENST00000274793.12:c.1136T= MANE Select ENSP00000274793.7:p.Val379=
NM_001168357.1:c.1136T= NP_001161829.1:p.Val379=
NM_001168357.2:c.1136T= NP_001161829.1:p.Val379=
NM_005084.3:c.1136T= NP_005075.3:p.Val379=
ENST00000274793.11:c.1136T= ENSP00000274793.7:p.Val379=
ENST00000537365.1:c.1136T= ENSP00000445666.1:p.Val379=
XM_005249408.3:c.1136T= XP_005249465.1:p.Val379=
XM_005249408.4:c.1136T= XP_005249465.1:p.Val379=
XR_001743639.2:n.1290T=
XR_002956305.1:n.3472T=