Canonical Allele Identifier: CA363937418
Community Standard Title: NM_005084.4(PLA2G7):c.593T>G (p.Ile198Arg)
Gene: PLA2G7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.46711566A>C , CM000668.2:g.46711566A>C GRCh38
NC_000006.11:g.46679303A>C , CM000668.1:g.46679303A>C GRCh37
NC_000006.10:g.46787262A>C NCBI36
NG_016204.1:g.29128T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005084.4:c.593T>G MANE Select NP_005075.3:p.Ile198Arg
ENST00000274793.12:c.593T>G MANE Select ENSP00000274793.7:p.Ile198Arg
NM_001168357.1:c.593T>G NP_001161829.1:p.Ile198Arg
NM_001168357.2:c.593T>G NP_001161829.1:p.Ile198Arg
NM_005084.3:c.593T>G NP_005075.3:p.Ile198Arg
ENST00000274793.11:c.593T>G ENSP00000274793.7:p.Ile198Arg
ENST00000537365.1:c.593T>G ENSP00000445666.1:p.Ile198Arg
XM_005249408.3:c.593T>G XP_005249465.1:p.Ile198Arg
XM_005249408.4:c.593T>G XP_005249465.1:p.Ile198Arg
XM_005249409.2:c.593T>G XP_005249466.1:p.Ile198Arg
XR_001743639.2:n.839T>G
XR_002956305.1:n.638T>G