Canonical Allele Identifier: CA377836456

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534542T>G (hg19) ; chr10:g.101774785T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774785T>G , CM000672.2:g.101774785T>G	GRCh38
NC_000010.10:g.103534542T>G , CM000672.1:g.103534542T>G	GRCh37
NC_000010.9:g.103524532T>G	NCBI36
NG_007151.1:g.6286A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.284A>C MANE Select	ENSP00000321797.2:p.Gln95Pro
ENST00000618991.5:c.-29A>C	ENSP00000484420.1:n.-29A>C
ENST00000344255.8:c.251A>C	ENSP00000340039.3:p.Gln84Pro
ENST00000320185.6:c.284A>C	ENSP00000321797.2:p.Gln95Pro
ENST00000344255.7:c.251A>C	ENSP00000340039.3:p.Gln84Pro
ENST00000346714.7:c.164A>C	ENSP00000344306.3:p.Gln55Pro
ENST00000347978.2:c.197A>C	ENSP00000321945.2:p.Gln66Pro
ENST00000469792.6:c.*248A>C	ENSP00000473299.1:n.*248A>C
ENST00000485728.1:n.160A>C
ENST00000618991.4:c.-29A>C	ENSP00000484420.1:n.-29A>C
NM_001206389.1:c.-29A>C	NP_001193318.1:n.-29A>C
NM_006119.4:c.197A>C	NP_006110.1:p.Gln66Pro
NM_033163.3:c.284A>C	NP_149353.1:p.Gln95Pro
NM_033164.3:c.251A>C	NP_149354.1:p.Gln84Pro
NM_033165.3:c.164A>C	NP_149355.1:p.Gln55Pro
XM_011539509.1:c.206A>C	XP_011537811.1:p.Gln69Pro
NM_006119.5:c.197A>C	NP_006110.1:p.Gln66Pro
NM_033163.4:c.284A>C	NP_149353.1:p.Gln95Pro
NM_033164.4:c.251A>C	NP_149354.1:p.Gln84Pro
NM_033165.4:c.164A>C	NP_149355.1:p.Gln55Pro
NM_001206389.2:c.-29A>C	NP_001193318.1:n.-29A>C
NM_006119.6:c.197A>C	NP_006110.1:p.Gln66Pro
NM_033163.5:c.284A>C MANE Select	NP_149353.1:p.Gln95Pro
NM_033165.5:c.164A>C	NP_149355.1:p.Gln55Pro