Canonical Allele Identifier: CA377834374

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531260A>T (hg19) ; chr10:g.101771503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771503A>T , CM000672.2:g.101771503A>T	GRCh38
NC_000010.10:g.103531260A>T , CM000672.1:g.103531260A>T	GRCh37
NC_000010.9:g.103521250A>T	NCBI36
NG_007151.1:g.9568T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.404T>A MANE Select	ENSP00000321797.2:p.Leu135His
ENST00000618991.5:c.92T>A	ENSP00000484420.1:p.Leu31His
ENST00000344255.8:c.371T>A	ENSP00000340039.3:p.Leu124His
ENST00000320185.6:c.404T>A	ENSP00000321797.2:p.Leu135His
ENST00000344255.7:c.371T>A	ENSP00000340039.3:p.Leu124His
ENST00000346714.7:c.284T>A	ENSP00000344306.3:p.Leu95His
ENST00000347978.2:c.317T>A	ENSP00000321945.2:p.Leu106His
ENST00000469792.6:c.*368T>A	ENSP00000473299.1:n.*368T>A
ENST00000485728.1:n.280T>A
ENST00000618991.4:c.92T>A	ENSP00000484420.1:p.Leu31His
NM_001206389.1:c.92T>A	NP_001193318.1:p.Leu31His
NM_006119.4:c.317T>A	NP_006110.1:p.Leu106His
NM_033163.3:c.404T>A	NP_149353.1:p.Leu135His
NM_033164.3:c.371T>A	NP_149354.1:p.Leu124His
NM_033165.3:c.284T>A	NP_149355.1:p.Leu95His
XM_011539509.1:c.326T>A	XP_011537811.1:p.Leu109His
XR_946251.1:n.284A>T
XR_946252.1:n.215A>T
XR_946253.1:n.213A>T
XR_946252.2:n.305A>T
XR_946253.2:n.303A>T
NM_006119.5:c.317T>A	NP_006110.1:p.Leu106His
NM_033163.4:c.404T>A	NP_149353.1:p.Leu135His
NM_033164.4:c.371T>A	NP_149354.1:p.Leu124His
NM_033165.4:c.284T>A	NP_149355.1:p.Leu95His
NM_001206389.2:c.92T>A	NP_001193318.1:p.Leu31His
NM_006119.6:c.317T>A	NP_006110.1:p.Leu106His
NM_033163.5:c.404T>A MANE Select	NP_149353.1:p.Leu135His
NM_033165.5:c.284T>A	NP_149355.1:p.Leu95His