Canonical Allele Identifier: CA377836613

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534554C>A (hg19) ; chr10:g.101774797C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774797C>A , CM000672.2:g.101774797C>A	GRCh38
NC_000010.10:g.103534554C>A , CM000672.1:g.103534554C>A	GRCh37
NC_000010.9:g.103524544C>A	NCBI36
NG_007151.1:g.6274G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.272G>T MANE Select	ENSP00000321797.2:p.Gly91Val
ENST00000618991.5:c.-41G>T	ENSP00000484420.1:n.-41G>T
ENST00000344255.8:c.239G>T	ENSP00000340039.3:p.Gly80Val
ENST00000320185.6:c.272G>T	ENSP00000321797.2:p.Gly91Val
ENST00000344255.7:c.239G>T	ENSP00000340039.3:p.Gly80Val
ENST00000346714.7:c.152G>T	ENSP00000344306.3:p.Gly51Val
ENST00000347978.2:c.185G>T	ENSP00000321945.2:p.Gly62Val
ENST00000469792.6:c.*236G>T	ENSP00000473299.1:n.*236G>T
ENST00000485728.1:n.148G>T
ENST00000618991.4:c.-41G>T	ENSP00000484420.1:n.-41G>T
NM_001206389.1:c.-41G>T	NP_001193318.1:n.-41G>T
NM_006119.4:c.185G>T	NP_006110.1:p.Gly62Val
NM_033163.3:c.272G>T	NP_149353.1:p.Gly91Val
NM_033164.3:c.239G>T	NP_149354.1:p.Gly80Val
NM_033165.3:c.152G>T	NP_149355.1:p.Gly51Val
XM_011539509.1:c.194G>T	XP_011537811.1:p.Gly65Val
NM_006119.5:c.185G>T	NP_006110.1:p.Gly62Val
NM_033163.4:c.272G>T	NP_149353.1:p.Gly91Val
NM_033164.4:c.239G>T	NP_149354.1:p.Gly80Val
NM_033165.4:c.152G>T	NP_149355.1:p.Gly51Val
NM_001206389.2:c.-41G>T	NP_001193318.1:n.-41G>T
NM_006119.6:c.185G>T	NP_006110.1:p.Gly62Val
NM_033163.5:c.272G>T MANE Select	NP_149353.1:p.Gly91Val
NM_033165.5:c.152G>T	NP_149355.1:p.Gly51Val