Canonical Allele Identifier: CA377836942

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534587A>T (hg19) ; chr10:g.101774830A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774830A>T , CM000672.2:g.101774830A>T	GRCh38
NC_000010.10:g.103534587A>T , CM000672.1:g.103534587A>T	GRCh37
NC_000010.9:g.103524577A>T	NCBI36
NG_007151.1:g.6241T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.239T>A MANE Select	ENSP00000321797.2:p.Ile80Asn
ENST00000618991.5:c.-74T>A	ENSP00000484420.1:n.-74T>A
ENST00000344255.8:c.206T>A	ENSP00000340039.3:p.Ile69Asn
ENST00000320185.6:c.239T>A	ENSP00000321797.2:p.Ile80Asn
ENST00000344255.7:c.206T>A	ENSP00000340039.3:p.Ile69Asn
ENST00000346714.7:c.119T>A	ENSP00000344306.3:p.Ile40Asn
ENST00000347978.2:c.152T>A	ENSP00000321945.2:p.Ile51Asn
ENST00000469792.6:c.*203T>A	ENSP00000473299.1:n.*203T>A
ENST00000485728.1:n.115T>A
ENST00000618991.4:c.-74T>A	ENSP00000484420.1:n.-74T>A
NM_001206389.1:c.-74T>A	NP_001193318.1:n.-74T>A
NM_006119.4:c.152T>A	NP_006110.1:p.Ile51Asn
NM_033163.3:c.239T>A	NP_149353.1:p.Ile80Asn
NM_033164.3:c.206T>A	NP_149354.1:p.Ile69Asn
NM_033165.3:c.119T>A	NP_149355.1:p.Ile40Asn
XM_011539509.1:c.161T>A	XP_011537811.1:p.Ile54Asn
NM_006119.5:c.152T>A	NP_006110.1:p.Ile51Asn
NM_033163.4:c.239T>A	NP_149353.1:p.Ile80Asn
NM_033164.4:c.206T>A	NP_149354.1:p.Ile69Asn
NM_033165.4:c.119T>A	NP_149355.1:p.Ile40Asn
NM_001206389.2:c.-74T>A	NP_001193318.1:n.-74T>A
NM_006119.6:c.152T>A	NP_006110.1:p.Ile51Asn
NM_033163.5:c.239T>A MANE Select	NP_149353.1:p.Ile80Asn
NM_033165.5:c.119T>A	NP_149355.1:p.Ile40Asn