Canonical Allele Identifier: CA2678108310
Gene: EGFL8 HGNC NCBI
PPT2-EGFL8 HGNC NCBI

Linked Data

gnomAD v4: 6-32164675-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32164675G>A , CM000668.2:g.32164675G>A GRCh38
NC_000006.11:g.32132452G>A , CM000668.1:g.32132452G>A GRCh37
NC_000006.10:g.32240430G>A NCBI36
NG_042283.1:g.16224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333845.11:c.-29+18G>A (EGFL8) MANE Select ENSP00000333380.6:n.-29+18G>A
ENST00000333845.10:c.-29+18G>A (EGFL8) ENSP00000333380.6:n.-29+18G>A
ENST00000395512.5:c.-35G>A (EGFL8) ENSP00000378888.1:n.-35G>A
ENST00000421600.2:c.321G>A (PPT2-EGFL8)
ENST00000422437.5:c.844+18G>A (PPT2-EGFL8) ENSP00000457534.1:n.844+18G>A
ENST00000428388.6:c.844+18G>A (PPT2-EGFL8) ENSP00000455087.1:n.844+18G>A
ENST00000432129.1:c.-35G>A (EGFL8) ENSP00000401694.1:n.-35G>A
ENST00000453656.6:n.975+18G>A (PPT2-EGFL8)
ENST00000479001.2:n.829+18G>A (PPT2-EGFL8)
ENST00000583227.5:c.*396+18G>A (PPT2-EGFL8) ENSP00000461909.1:n.*396+18G>A
ENST00000585246.5:c.*318-1463G>A (PPT2-EGFL8) ENSP00000463570.1:n.*318-1463G>A
NM_030652.3:c.-29+18G>A (EGFL8) NP_085155.1:n.-29+18G>A
NR_037860.1:n.71G>A (EGFL8)
NR_037861.1:n.1258+18G>A (PPT2-EGFL8)
NM_030652.4:c.-29+18G>A (EGFL8) MANE Select NP_085155.1:n.-29+18G>A
NR_037860.2:n.81G>A (EGFL8)