Canonical Allele Identifier: CA377834486

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531296C>A (hg19) ; chr10:g.101771539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771539C>A , CM000672.2:g.101771539C>A	GRCh38
NC_000010.10:g.103531296C>A , CM000672.1:g.103531296C>A	GRCh37
NC_000010.9:g.103521286C>A	NCBI36
NG_007151.1:g.9532G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.368G>T MANE Select	ENSP00000321797.2:p.Gly123Val
ENST00000618991.5:c.56G>T	ENSP00000484420.1:p.Gly19Val
ENST00000344255.8:c.335G>T	ENSP00000340039.3:p.Gly112Val
ENST00000320185.6:c.368G>T	ENSP00000321797.2:p.Gly123Val
ENST00000344255.7:c.335G>T	ENSP00000340039.3:p.Gly112Val
ENST00000346714.7:c.248G>T	ENSP00000344306.3:p.Gly83Val
ENST00000347978.2:c.281G>T	ENSP00000321945.2:p.Gly94Val
ENST00000469792.6:c.*332G>T	ENSP00000473299.1:n.*332G>T
ENST00000485728.1:n.244G>T
ENST00000618991.4:c.56G>T	ENSP00000484420.1:p.Gly19Val
NM_001206389.1:c.56G>T	NP_001193318.1:p.Gly19Val
NM_006119.4:c.281G>T	NP_006110.1:p.Gly94Val
NM_033163.3:c.368G>T	NP_149353.1:p.Gly123Val
NM_033164.3:c.335G>T	NP_149354.1:p.Gly112Val
NM_033165.3:c.248G>T	NP_149355.1:p.Gly83Val
XM_011539509.1:c.290G>T	XP_011537811.1:p.Gly97Val
XR_946251.1:n.320C>A
XR_946252.1:n.251C>A
XR_946253.1:n.249C>A
XR_946252.2:n.341C>A
XR_946253.2:n.339C>A
NM_006119.5:c.281G>T	NP_006110.1:p.Gly94Val
NM_033163.4:c.368G>T	NP_149353.1:p.Gly123Val
NM_033164.4:c.335G>T	NP_149354.1:p.Gly112Val
NM_033165.4:c.248G>T	NP_149355.1:p.Gly83Val
NM_001206389.2:c.56G>T	NP_001193318.1:p.Gly19Val
NM_006119.6:c.281G>T	NP_006110.1:p.Gly94Val
NM_033163.5:c.368G>T MANE Select	NP_149353.1:p.Gly123Val
NM_033165.5:c.248G>T	NP_149355.1:p.Gly83Val