Canonical Allele Identifier: CA449704202
Gene: EGFL8 HGNC NCBI
PPT2-EGFL8 HGNC NCBI

Linked Data

gnomAD v4: 6-32164593-C-A
MyVariant Identifiers: chr6:g.32132370C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164593C>A , CM000668.2:g.32164593C>A GRCh38
NC_000006.11:g.32132370C>A , CM000668.1:g.32132370C>A GRCh37
NC_000006.10:g.32240348C>A NCBI36
NG_042283.1:g.16142C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333845.10:c.-93C>A (EGFL8) ENSP00000333380.6:n.-93C>A
ENST00000421600.2:c.239C>A (PPT2-EGFL8)
ENST00000422437.5:c.780C>A (PPT2-EGFL8) ENSP00000457534.1:p.Thr260=
ENST00000428388.6:c.780C>A (PPT2-EGFL8) ENSP00000455087.1:p.Thr260=
ENST00000453656.6:n.911C>A (PPT2-EGFL8)
ENST00000479001.2:n.765C>A (PPT2-EGFL8)
ENST00000583227.5:c.*332C>A (PPT2-EGFL8) ENSP00000461909.1:n.*332C>A
ENST00000585246.5:c.*318-1545C>A (PPT2-EGFL8) ENSP00000463570.1:n.*318-1545C>A
NR_037861.1:n.1194C>A (PPT2-EGFL8)