Canonical Allele Identifier: CA377836863

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534576G>A (hg19) ; chr10:g.101774819G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774819G>A , CM000672.2:g.101774819G>A	GRCh38
NC_000010.10:g.103534576G>A , CM000672.1:g.103534576G>A	GRCh37
NC_000010.9:g.103524566G>A	NCBI36
NG_007151.1:g.6252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.250C>T MANE Select	ENSP00000321797.2:p.Gln84Ter
ENST00000618991.5:c.-63C>T	ENSP00000484420.1:n.-63C>T
ENST00000344255.8:c.217C>T	ENSP00000340039.3:p.Gln73Ter
ENST00000320185.6:c.250C>T	ENSP00000321797.2:p.Gln84Ter
ENST00000344255.7:c.217C>T	ENSP00000340039.3:p.Gln73Ter
ENST00000346714.7:c.130C>T	ENSP00000344306.3:p.Gln44Ter
ENST00000347978.2:c.163C>T	ENSP00000321945.2:p.Gln55Ter
ENST00000469792.6:c.*214C>T	ENSP00000473299.1:n.*214C>T
ENST00000485728.1:n.126C>T
ENST00000618991.4:c.-63C>T	ENSP00000484420.1:n.-63C>T
NM_001206389.1:c.-63C>T	NP_001193318.1:n.-63C>T
NM_006119.4:c.163C>T	NP_006110.1:p.Gln55Ter
NM_033163.3:c.250C>T	NP_149353.1:p.Gln84Ter
NM_033164.3:c.217C>T	NP_149354.1:p.Gln73Ter
NM_033165.3:c.130C>T	NP_149355.1:p.Gln44Ter
XM_011539509.1:c.172C>T	XP_011537811.1:p.Gln58Ter
NM_006119.5:c.163C>T	NP_006110.1:p.Gln55Ter
NM_033163.4:c.250C>T	NP_149353.1:p.Gln84Ter
NM_033164.4:c.217C>T	NP_149354.1:p.Gln73Ter
NM_033165.4:c.130C>T	NP_149355.1:p.Gln44Ter
NM_001206389.2:c.-63C>T	NP_001193318.1:n.-63C>T
NM_006119.6:c.163C>T	NP_006110.1:p.Gln55Ter
NM_033163.5:c.250C>T MANE Select	NP_149353.1:p.Gln84Ter
NM_033165.5:c.130C>T	NP_149355.1:p.Gln44Ter