Canonical Allele Identifier: CA377834476

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531291T>A (hg19) ; chr10:g.101771534T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771534T>A , CM000672.2:g.101771534T>A	GRCh38
NC_000010.10:g.103531291T>A , CM000672.1:g.103531291T>A	GRCh37
NC_000010.9:g.103521281T>A	NCBI36
NG_007151.1:g.9537A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.373A>T MANE Select	ENSP00000321797.2:p.Arg125Ter
ENST00000618991.5:c.61A>T	ENSP00000484420.1:p.Arg21Ter
ENST00000344255.8:c.340A>T	ENSP00000340039.3:p.Arg114Ter
ENST00000320185.6:c.373A>T	ENSP00000321797.2:p.Arg125Ter
ENST00000344255.7:c.340A>T	ENSP00000340039.3:p.Arg114Ter
ENST00000346714.7:c.253A>T	ENSP00000344306.3:p.Arg85Ter
ENST00000347978.2:c.286A>T	ENSP00000321945.2:p.Arg96Ter
ENST00000469792.6:c.*337A>T	ENSP00000473299.1:n.*337A>T
ENST00000485728.1:n.249A>T
ENST00000618991.4:c.61A>T	ENSP00000484420.1:p.Arg21Ter
NM_001206389.1:c.61A>T	NP_001193318.1:p.Arg21Ter
NM_006119.4:c.286A>T	NP_006110.1:p.Arg96Ter
NM_033163.3:c.373A>T	NP_149353.1:p.Arg125Ter
NM_033164.3:c.340A>T	NP_149354.1:p.Arg114Ter
NM_033165.3:c.253A>T	NP_149355.1:p.Arg85Ter
XM_011539509.1:c.295A>T	XP_011537811.1:p.Arg99Ter
XR_946251.1:n.315T>A
XR_946252.1:n.246T>A
XR_946253.1:n.244T>A
XR_946252.2:n.336T>A
XR_946253.2:n.334T>A
NM_006119.5:c.286A>T	NP_006110.1:p.Arg96Ter
NM_033163.4:c.373A>T	NP_149353.1:p.Arg125Ter
NM_033164.4:c.340A>T	NP_149354.1:p.Arg114Ter
NM_033165.4:c.253A>T	NP_149355.1:p.Arg85Ter
NM_001206389.2:c.61A>T	NP_001193318.1:p.Arg21Ter
NM_006119.6:c.286A>T	NP_006110.1:p.Arg96Ter
NM_033163.5:c.373A>T MANE Select	NP_149353.1:p.Arg125Ter
NM_033165.5:c.253A>T	NP_149355.1:p.Arg85Ter