Canonical Allele Identifier: CA2838318211

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774748dup , CM000672.2:g.101774748dup	GRCh38
NC_000010.10:g.103534505dup , CM000672.1:g.103534505dup	GRCh37
NC_000010.9:g.103524495dup	NCBI36
NG_007151.1:g.6324dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.322dup MANE Select	ENSP00000321797.2:p.Asp108GlyfsTer?
ENST00000618991.5:c.10dup	ENSP00000484420.1:p.Asp4GlyfsTer?
ENST00000344255.8:c.289dup	ENSP00000340039.3:p.Asp97GlyfsTer?
ENST00000320185.6:c.322dup	ENSP00000321797.2:p.Asp108GlyfsTer?
ENST00000344255.7:c.289dup	ENSP00000340039.3:p.Asp97GlyfsTer?
ENST00000346714.7:c.202dup	ENSP00000344306.3:p.Asp68GlyfsTer?
ENST00000347978.2:c.235dup	ENSP00000321945.2:p.Asp79GlyfsTer?
ENST00000469792.6:c.*286dup	ENSP00000473299.1:n.*286dup
ENST00000485728.1:n.198dup
ENST00000618991.4:c.10dup	ENSP00000484420.1:p.Asp4GlyfsTer?
NM_001206389.1:c.10dup	NP_001193318.1:p.Asp4GlyfsTer?
NM_006119.4:c.235dup	NP_006110.1:p.Asp79GlyfsTer?
NM_033163.3:c.322dup	NP_149353.1:p.Asp108GlyfsTer?
NM_033164.3:c.289dup	NP_149354.1:p.Asp97GlyfsTer?
NM_033165.3:c.202dup	NP_149355.1:p.Asp68GlyfsTer?
XM_011539509.1:c.244dup	XP_011537811.1:p.Asp82GlyfsTer?
NM_006119.5:c.235dup	NP_006110.1:p.Asp79GlyfsTer?
NM_033163.4:c.322dup	NP_149353.1:p.Asp108GlyfsTer?
NM_033164.4:c.289dup	NP_149354.1:p.Asp97GlyfsTer?
NM_033165.4:c.202dup	NP_149355.1:p.Asp68GlyfsTer?
NM_001206389.2:c.10dup	NP_001193318.1:p.Asp4GlyfsTer?
NM_006119.6:c.235dup	NP_006110.1:p.Asp79GlyfsTer?
NM_033163.5:c.322dup MANE Select	NP_149353.1:p.Asp108GlyfsTer?
NM_033165.5:c.202dup	NP_149355.1:p.Asp68GlyfsTer?