Canonical Allele Identifier: CA136901504

Gene: EGFL8 PPT2-EGFL8

Linked Data

• dbSNP Id: rs1032885287
• gnomAD v3: 6-32164705-T-C
• gnomAD v4: 6-32164705-T-C
• MyVariant Identifiers: chr6:g.32132482T>C (hg19) ; chr6:g.32164705T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32164705T>C , CM000668.2:g.32164705T>C	GRCh38
NC_000006.11:g.32132482T>C , CM000668.1:g.32132482T>C	GRCh37
NC_000006.10:g.32240460T>C	NCBI36
NG_042283.1:g.16254T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333845.11:c.-29+48T>C (EGFL8) MANE Select	ENSP00000333380.6:n.-29+48T>C
ENST00000333845.10:c.-29+48T>C (EGFL8)	ENSP00000333380.6:n.-29+48T>C
ENST00000395512.5:c.-29+24T>C (EGFL8)	ENSP00000378888.1:n.-29+24T>C
ENST00000421600.2:c.327+24T>C (PPT2-EGFL8)
ENST00000422437.5:c.844+48T>C (PPT2-EGFL8)	ENSP00000457534.1:n.844+48T>C
ENST00000428388.6:c.844+48T>C (PPT2-EGFL8)	ENSP00000455087.1:n.844+48T>C
ENST00000432129.1:c.-29+24T>C (EGFL8)	ENSP00000401694.1:n.-29+24T>C
ENST00000453656.6:n.975+48T>C (PPT2-EGFL8)
ENST00000479001.2:n.829+48T>C (PPT2-EGFL8)
ENST00000583227.5:c.*396+48T>C (PPT2-EGFL8)	ENSP00000461909.1:n.*396+48T>C
ENST00000585246.5:c.*318-1433T>C (PPT2-EGFL8)	ENSP00000463570.1:n.*318-1433T>C
NM_030652.3:c.-29+48T>C (EGFL8)	NP_085155.1:n.-29+48T>C
NR_037860.1:n.77+24T>C (EGFL8)
NR_037861.1:n.1258+48T>C (PPT2-EGFL8)
NM_030652.4:c.-29+48T>C (EGFL8) MANE Select	NP_085155.1:n.-29+48T>C
NR_037860.2:n.87+24T>C (EGFL8)