Canonical Allele Identifier: CA1087517368
Gene: EGFL8 HGNC NCBI
PPT2-EGFL8 HGNC NCBI

Linked Data

dbSNP Id: rs1784368839
gnomAD v3: 6-32164754-G-A
gnomAD v4: 6-32164754-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164754G>A , CM000668.2:g.32164754G>A GRCh38
NC_000006.11:g.32132531G>A , CM000668.1:g.32132531G>A GRCh37
NC_000006.10:g.32240509G>A NCBI36
NG_042283.1:g.16303G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333845.11:c.-29+97G>A (EGFL8) MANE Select ENSP00000333380.6:n.-29+97G>A
ENST00000333845.10:c.-29+97G>A (EGFL8) ENSP00000333380.6:n.-29+97G>A
ENST00000395512.5:c.-29+73G>A (EGFL8) ENSP00000378888.1:n.-29+73G>A
ENST00000421600.2:c.327+73G>A (PPT2-EGFL8)
ENST00000422437.5:c.844+97G>A (PPT2-EGFL8) ENSP00000457534.1:n.844+97G>A
ENST00000428388.6:c.844+97G>A (PPT2-EGFL8) ENSP00000455087.1:n.844+97G>A
ENST00000432129.1:c.-29+73G>A (EGFL8) ENSP00000401694.1:n.-29+73G>A
ENST00000453656.6:n.975+97G>A (PPT2-EGFL8)
ENST00000479001.2:n.829+97G>A (PPT2-EGFL8)
ENST00000583227.5:c.*396+97G>A (PPT2-EGFL8) ENSP00000461909.1:n.*396+97G>A
ENST00000585246.5:c.*318-1384G>A (PPT2-EGFL8) ENSP00000463570.1:n.*318-1384G>A
NM_030652.3:c.-29+97G>A (EGFL8) NP_085155.1:n.-29+97G>A
NR_037860.1:n.77+73G>A (EGFL8)
NR_037861.1:n.1258+97G>A (PPT2-EGFL8)
NM_030652.4:c.-29+97G>A (EGFL8) MANE Select NP_085155.1:n.-29+97G>A
NR_037860.2:n.87+73G>A (EGFL8)