Canonical Allele Identifier: CA449704177
Gene: EGFL8 HGNC NCBI
PPT2-EGFL8 HGNC NCBI

Linked Data

gnomAD v4: 6-32164588-C-A
MyVariant Identifiers: chr6:g.32132365C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164588C>A , CM000668.2:g.32164588C>A GRCh38
NC_000006.11:g.32132365C>A , CM000668.1:g.32132365C>A GRCh37
NC_000006.10:g.32240343C>A NCBI36
NG_042283.1:g.16137C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333845.10:c.-98C>A (EGFL8) ENSP00000333380.6:n.-98C>A
ENST00000421600.2:c.234C>A (PPT2-EGFL8)
ENST00000422437.5:c.775C>A (PPT2-EGFL8) ENSP00000457534.1:p.Pro259Thr
ENST00000428388.6:c.775C>A (PPT2-EGFL8) ENSP00000455087.1:p.Pro259Thr
ENST00000453656.6:n.906C>A (PPT2-EGFL8)
ENST00000479001.2:n.760C>A (PPT2-EGFL8)
ENST00000583227.5:c.*327C>A (PPT2-EGFL8) ENSP00000461909.1:n.*327C>A
ENST00000585246.5:c.*318-1550C>A (PPT2-EGFL8) ENSP00000463570.1:n.*318-1550C>A
NR_037861.1:n.1189C>A (PPT2-EGFL8)