Canonical Allele Identifier: CA377836938

Gene: FGF8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.239T>C MANE Select	ENSP00000321797.2:p.Ile80Thr
ENST00000618991.5:c.-74T>C	ENSP00000484420.1:n.-74T>C
ENST00000344255.8:c.206T>C	ENSP00000340039.3:p.Ile69Thr
ENST00000320185.6:c.239T>C	ENSP00000321797.2:p.Ile80Thr
ENST00000344255.7:c.206T>C	ENSP00000340039.3:p.Ile69Thr
ENST00000346714.7:c.119T>C	ENSP00000344306.3:p.Ile40Thr
ENST00000347978.2:c.152T>C	ENSP00000321945.2:p.Ile51Thr
ENST00000469792.6:c.*203T>C	ENSP00000473299.1:n.*203T>C
ENST00000485728.1:n.115T>C
ENST00000618991.4:c.-74T>C	ENSP00000484420.1:n.-74T>C
NM_001206389.1:c.-74T>C	NP_001193318.1:n.-74T>C
NM_006119.4:c.152T>C	NP_006110.1:p.Ile51Thr
NM_033163.3:c.239T>C	NP_149353.1:p.Ile80Thr
NM_033164.3:c.206T>C	NP_149354.1:p.Ile69Thr
NM_033165.3:c.119T>C	NP_149355.1:p.Ile40Thr
XM_011539509.1:c.161T>C	XP_011537811.1:p.Ile54Thr
NM_006119.5:c.152T>C	NP_006110.1:p.Ile51Thr
NM_033163.4:c.239T>C	NP_149353.1:p.Ile80Thr
NM_033164.4:c.206T>C	NP_149354.1:p.Ile69Thr
NM_033165.4:c.119T>C	NP_149355.1:p.Ile40Thr
NM_001206389.2:c.-74T>C	NP_001193318.1:n.-74T>C
NM_006119.6:c.152T>C	NP_006110.1:p.Ile51Thr
NM_033163.5:c.239T>C MANE Select	NP_149353.1:p.Ile80Thr
NM_033165.5:c.119T>C	NP_149355.1:p.Ile40Thr