Canonical Allele Identifier: CA377834455

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531287A>G (hg19) ; chr10:g.101771530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771530A>G , CM000672.2:g.101771530A>G	GRCh38
NC_000010.10:g.103531287A>G , CM000672.1:g.103531287A>G	GRCh37
NC_000010.9:g.103521277A>G	NCBI36
NG_007151.1:g.9541T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.377T>C MANE Select	ENSP00000321797.2:p.Val126Ala
ENST00000618991.5:c.65T>C	ENSP00000484420.1:p.Val22Ala
ENST00000344255.8:c.344T>C	ENSP00000340039.3:p.Val115Ala
ENST00000320185.6:c.377T>C	ENSP00000321797.2:p.Val126Ala
ENST00000344255.7:c.344T>C	ENSP00000340039.3:p.Val115Ala
ENST00000346714.7:c.257T>C	ENSP00000344306.3:p.Val86Ala
ENST00000347978.2:c.290T>C	ENSP00000321945.2:p.Val97Ala
ENST00000469792.6:c.*341T>C	ENSP00000473299.1:n.*341T>C
ENST00000485728.1:n.253T>C
ENST00000618991.4:c.65T>C	ENSP00000484420.1:p.Val22Ala
NM_001206389.1:c.65T>C	NP_001193318.1:p.Val22Ala
NM_006119.4:c.290T>C	NP_006110.1:p.Val97Ala
NM_033163.3:c.377T>C	NP_149353.1:p.Val126Ala
NM_033164.3:c.344T>C	NP_149354.1:p.Val115Ala
NM_033165.3:c.257T>C	NP_149355.1:p.Val86Ala
XM_011539509.1:c.299T>C	XP_011537811.1:p.Val100Ala
XR_946251.1:n.311A>G
XR_946252.1:n.242A>G
XR_946253.1:n.240A>G
XR_946252.2:n.332A>G
XR_946253.2:n.330A>G
NM_006119.5:c.290T>C	NP_006110.1:p.Val97Ala
NM_033163.4:c.377T>C	NP_149353.1:p.Val126Ala
NM_033164.4:c.344T>C	NP_149354.1:p.Val115Ala
NM_033165.4:c.257T>C	NP_149355.1:p.Val86Ala
NM_001206389.2:c.65T>C	NP_001193318.1:p.Val22Ala
NM_006119.6:c.290T>C	NP_006110.1:p.Val97Ala
NM_033163.5:c.377T>C MANE Select	NP_149353.1:p.Val126Ala
NM_033165.5:c.257T>C	NP_149355.1:p.Val86Ala