Canonical Allele Identifier: CA449704377

Gene: EGFL8 PPT2-EGFL8

Linked Data

• gnomAD v4: 6-32164640-C-G
• MyVariant Identifiers: chr6:g.32132417C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32164640C>G , CM000668.2:g.32164640C>G	GRCh38
NC_000006.11:g.32132417C>G , CM000668.1:g.32132417C>G	GRCh37
NC_000006.10:g.32240395C>G	NCBI36
NG_042283.1:g.16189C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333845.11:c.-46C>G (EGFL8) MANE Select	ENSP00000333380.6:n.-46C>G
ENST00000333845.10:c.-46C>G (EGFL8)	ENSP00000333380.6:n.-46C>G
ENST00000395512.5:c.-70C>G (EGFL8)	ENSP00000378888.1:n.-70C>G
ENST00000421600.2:c.286C>G (PPT2-EGFL8)
ENST00000422437.5:c.827C>G (PPT2-EGFL8)	ENSP00000457534.1:p.Pro276Arg
ENST00000428388.6:c.827C>G (PPT2-EGFL8)	ENSP00000455087.1:p.Pro276Arg
ENST00000453656.6:n.958C>G (PPT2-EGFL8)
ENST00000479001.2:n.812C>G (PPT2-EGFL8)
ENST00000583227.5:c.*379C>G (PPT2-EGFL8)	ENSP00000461909.1:n.*379C>G
ENST00000585246.5:c.*318-1498C>G (PPT2-EGFL8)	ENSP00000463570.1:n.*318-1498C>G
NM_030652.3:c.-46C>G (EGFL8)	NP_085155.1:n.-46C>G
NR_037860.1:n.36C>G (EGFL8)
NR_037861.1:n.1241C>G (PPT2-EGFL8)
NM_030652.4:c.-46C>G (EGFL8) MANE Select	NP_085155.1:n.-46C>G
NR_037860.2:n.46C>G (EGFL8)