Canonical Allele Identifier: CA470996390

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534649A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774892A>T , CM000672.2:g.101774892A>T	GRCh38
NC_000010.10:g.103534649A>T , CM000672.1:g.103534649A>T	GRCh37
NC_000010.9:g.103524639A>T	NCBI36
NG_007151.1:g.6179T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.177T>A MANE Select	ENSP00000321797.2:p.Pro59=
ENST00000618991.5:c.-123-13T>A	ENSP00000484420.1:n.-123-13T>A
ENST00000344255.8:c.157-13T>A	ENSP00000340039.3:n.157-13T>A
ENST00000320185.6:c.177T>A	ENSP00000321797.2:p.Pro59=
ENST00000344255.7:c.157-13T>A	ENSP00000340039.3:n.157-13T>A
ENST00000346714.7:c.70-13T>A	ENSP00000344306.3:n.70-13T>A
ENST00000347978.2:c.90T>A	ENSP00000321945.2:p.Pro30=
ENST00000469792.6:c.*154-13T>A	ENSP00000473299.1:n.*154-13T>A
ENST00000485728.1:n.53T>A
ENST00000618991.4:c.-123-13T>A	ENSP00000484420.1:n.-123-13T>A
NM_001206389.1:c.-123-13T>A	NP_001193318.1:n.-123-13T>A
NM_006119.4:c.90T>A	NP_006110.1:p.Pro30=
NM_033163.3:c.177T>A	NP_149353.1:p.Pro59=
NM_033164.3:c.157-13T>A	NP_149354.1:n.157-13T>A
NM_033165.3:c.70-13T>A	NP_149355.1:n.70-13T>A
XM_011539509.1:c.99T>A	XP_011537811.1:p.Pro33=
NM_006119.5:c.90T>A	NP_006110.1:p.Pro30=
NM_033163.4:c.177T>A	NP_149353.1:p.Pro59=
NM_033164.4:c.157-13T>A	NP_149354.1:n.157-13T>A
NM_033165.4:c.70-13T>A	NP_149355.1:n.70-13T>A
NM_001206389.2:c.-123-13T>A	NP_001193318.1:n.-123-13T>A
NM_006119.6:c.90T>A	NP_006110.1:p.Pro30=
NM_033163.5:c.177T>A MANE Select	NP_149353.1:p.Pro59=
NM_033165.5:c.70-13T>A	NP_149355.1:n.70-13T>A