Canonical Allele Identifier: CA377837122

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534609C>A (hg19) ; chr10:g.101774852C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774852C>A , CM000672.2:g.101774852C>A	GRCh38
NC_000010.10:g.103534609C>A , CM000672.1:g.103534609C>A	GRCh37
NC_000010.9:g.103524599C>A	NCBI36
NG_007151.1:g.6219G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.217G>T MANE Select	ENSP00000321797.2:p.Asp73Tyr
ENST00000618991.5:c.-96G>T	ENSP00000484420.1:n.-96G>T
ENST00000344255.8:c.184G>T	ENSP00000340039.3:p.Asp62Tyr
ENST00000320185.6:c.217G>T	ENSP00000321797.2:p.Asp73Tyr
ENST00000344255.7:c.184G>T	ENSP00000340039.3:p.Asp62Tyr
ENST00000346714.7:c.97G>T	ENSP00000344306.3:p.Asp33Tyr
ENST00000347978.2:c.130G>T	ENSP00000321945.2:p.Asp44Tyr
ENST00000469792.6:c.*181G>T	ENSP00000473299.1:n.*181G>T
ENST00000485728.1:n.93G>T
ENST00000618991.4:c.-96G>T	ENSP00000484420.1:n.-96G>T
NM_001206389.1:c.-96G>T	NP_001193318.1:n.-96G>T
NM_006119.4:c.130G>T	NP_006110.1:p.Asp44Tyr
NM_033163.3:c.217G>T	NP_149353.1:p.Asp73Tyr
NM_033164.3:c.184G>T	NP_149354.1:p.Asp62Tyr
NM_033165.3:c.97G>T	NP_149355.1:p.Asp33Tyr
XM_011539509.1:c.139G>T	XP_011537811.1:p.Asp47Tyr
NM_006119.5:c.130G>T	NP_006110.1:p.Asp44Tyr
NM_033163.4:c.217G>T	NP_149353.1:p.Asp73Tyr
NM_033164.4:c.184G>T	NP_149354.1:p.Asp62Tyr
NM_033165.4:c.97G>T	NP_149355.1:p.Asp33Tyr
NM_001206389.2:c.-96G>T	NP_001193318.1:n.-96G>T
NM_006119.6:c.130G>T	NP_006110.1:p.Asp44Tyr
NM_033163.5:c.217G>T MANE Select	NP_149353.1:p.Asp73Tyr
NM_033165.5:c.97G>T	NP_149355.1:p.Asp33Tyr