Canonical Allele Identifier: CA1626046287
Community Standard Title: NM_005084.4(PLA2G7):c.835G= (p.Val279=)
Gene: PLA2G7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.46709361C= , CM000668.2:g.46709361C= GRCh38
NC_000006.11:g.46677098C= , CM000668.1:g.46677098C= GRCh37
NC_000006.10:g.46785057C= NCBI36
NG_016204.1:g.31333G=

Transcript Alleles

HGVS Amino-acid Change
NM_005084.4:c.835G= MANE Select NP_005075.3:p.Val279=
ENST00000274793.12:c.835G= MANE Select ENSP00000274793.7:p.Val279=
NM_001168357.1:c.835G= NP_001161829.1:p.Val279=
NM_001168357.2:c.835G= NP_001161829.1:p.Val279=
NM_005084.3:c.835G= NP_005075.3:p.Val279=
ENST00000274793.11:c.835G= ENSP00000274793.7:p.Val279=
ENST00000537365.1:c.835G= ENSP00000445666.1:p.Val279=
XM_005249408.3:c.835G= XP_005249465.1:p.Val279=
XM_005249408.4:c.835G= XP_005249465.1:p.Val279=
XM_005249409.2:c.777+1184G= XP_005249466.1:n.777+1184G=
XR_001743639.2:n.1023+1184G=
XR_002956305.1:n.2006G=