Canonical Allele Identifier: CA377837113

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534608T>A (hg19) ; chr10:g.101774851T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774851T>A , CM000672.2:g.101774851T>A	GRCh38
NC_000010.10:g.103534608T>A , CM000672.1:g.103534608T>A	GRCh37
NC_000010.9:g.103524598T>A	NCBI36
NG_007151.1:g.6220A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.218A>T MANE Select	ENSP00000321797.2:p.Asp73Val
ENST00000618991.5:c.-95A>T	ENSP00000484420.1:n.-95A>T
ENST00000344255.8:c.185A>T	ENSP00000340039.3:p.Asp62Val
ENST00000320185.6:c.218A>T	ENSP00000321797.2:p.Asp73Val
ENST00000344255.7:c.185A>T	ENSP00000340039.3:p.Asp62Val
ENST00000346714.7:c.98A>T	ENSP00000344306.3:p.Asp33Val
ENST00000347978.2:c.131A>T	ENSP00000321945.2:p.Asp44Val
ENST00000469792.6:c.*182A>T	ENSP00000473299.1:n.*182A>T
ENST00000485728.1:n.94A>T
ENST00000618991.4:c.-95A>T	ENSP00000484420.1:n.-95A>T
NM_001206389.1:c.-95A>T	NP_001193318.1:n.-95A>T
NM_006119.4:c.131A>T	NP_006110.1:p.Asp44Val
NM_033163.3:c.218A>T	NP_149353.1:p.Asp73Val
NM_033164.3:c.185A>T	NP_149354.1:p.Asp62Val
NM_033165.3:c.98A>T	NP_149355.1:p.Asp33Val
XM_011539509.1:c.140A>T	XP_011537811.1:p.Asp47Val
NM_006119.5:c.131A>T	NP_006110.1:p.Asp44Val
NM_033163.4:c.218A>T	NP_149353.1:p.Asp73Val
NM_033164.4:c.185A>T	NP_149354.1:p.Asp62Val
NM_033165.4:c.98A>T	NP_149355.1:p.Asp33Val
NM_001206389.2:c.-95A>T	NP_001193318.1:n.-95A>T
NM_006119.6:c.131A>T	NP_006110.1:p.Asp44Val
NM_033163.5:c.218A>T MANE Select	NP_149353.1:p.Asp73Val
NM_033165.5:c.98A>T	NP_149355.1:p.Asp33Val