Canonical Allele Identifier: CA1619449989

Gene: EGFL8 PPT2-EGFL8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32164662G= , CM000668.2:g.32164662G=	GRCh38
NC_000006.11:g.32132439G= , CM000668.1:g.32132439G=	GRCh37
NC_000006.10:g.32240417G=	NCBI36
NG_042283.1:g.16211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333845.11:c.-29+5G= (EGFL8) MANE Select	ENSP00000333380.6:n.-29+5G=
ENST00000333845.10:c.-29+5G= (EGFL8)	ENSP00000333380.6:n.-29+5G=
ENST00000395512.5:c.-48G= (EGFL8)	ENSP00000378888.1:n.-48G=
ENST00000421600.2:c.308G= (PPT2-EGFL8)
ENST00000422437.5:c.844+5G= (PPT2-EGFL8)	ENSP00000457534.1:n.844+5G=
ENST00000428388.6:c.844+5G= (PPT2-EGFL8)	ENSP00000455087.1:n.844+5G=
ENST00000432129.1:c.-48G= (EGFL8)	ENSP00000401694.1:n.-48G=
ENST00000453656.6:n.975+5G= (PPT2-EGFL8)
ENST00000479001.2:n.829+5G= (PPT2-EGFL8)
ENST00000583227.5:c.*396+5G= (PPT2-EGFL8)	ENSP00000461909.1:n.*396+5G=
ENST00000585246.5:c.*318-1476G= (PPT2-EGFL8)	ENSP00000463570.1:n.*318-1476G=
NM_030652.3:c.-29+5G= (EGFL8)	NP_085155.1:n.-29+5G=
NR_037860.1:n.58G= (EGFL8)
NR_037861.1:n.1258+5G= (PPT2-EGFL8)
NM_030652.4:c.-29+5G= (EGFL8) MANE Select	NP_085155.1:n.-29+5G=
NR_037860.2:n.68G= (EGFL8)