Canonical Allele Identifier: CA377834251

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531228T>G (hg19) ; chr10:g.101771471T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771471T>G , CM000672.2:g.101771471T>G	GRCh38
NC_000010.10:g.103531228T>G , CM000672.1:g.103531228T>G	GRCh37
NC_000010.9:g.103521218T>G	NCBI36
NG_007151.1:g.9600A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.436A>C MANE Select	ENSP00000321797.2:p.Ile146Leu
ENST00000618991.5:c.124A>C	ENSP00000484420.1:p.Ile42Leu
ENST00000344255.8:c.403A>C	ENSP00000340039.3:p.Ile135Leu
ENST00000320185.6:c.436A>C	ENSP00000321797.2:p.Ile146Leu
ENST00000344255.7:c.403A>C	ENSP00000340039.3:p.Ile135Leu
ENST00000346714.7:c.316A>C	ENSP00000344306.3:p.Ile106Leu
ENST00000347978.2:c.349A>C	ENSP00000321945.2:p.Ile117Leu
ENST00000469792.6:c.*400A>C	ENSP00000473299.1:n.*400A>C
ENST00000485728.1:n.312A>C
ENST00000618991.4:c.124A>C	ENSP00000484420.1:p.Ile42Leu
NM_001206389.1:c.124A>C	NP_001193318.1:p.Ile42Leu
NM_006119.4:c.349A>C	NP_006110.1:p.Ile117Leu
NM_033163.3:c.436A>C	NP_149353.1:p.Ile146Leu
NM_033164.3:c.403A>C	NP_149354.1:p.Ile135Leu
NM_033165.3:c.316A>C	NP_149355.1:p.Ile106Leu
XM_011539509.1:c.358A>C	XP_011537811.1:p.Ile120Leu
XR_946251.1:n.278-26T>G
XR_946252.1:n.209-26T>G
XR_946253.1:n.207-26T>G
XR_946252.2:n.299-26T>G
XR_946253.2:n.297-26T>G
NM_006119.5:c.349A>C	NP_006110.1:p.Ile117Leu
NM_033163.4:c.436A>C	NP_149353.1:p.Ile146Leu
NM_033164.4:c.403A>C	NP_149354.1:p.Ile135Leu
NM_033165.4:c.316A>C	NP_149355.1:p.Ile106Leu
NM_001206389.2:c.124A>C	NP_001193318.1:p.Ile42Leu
NM_006119.6:c.349A>C	NP_006110.1:p.Ile117Leu
NM_033163.5:c.436A>C MANE Select	NP_149353.1:p.Ile146Leu
NM_033165.5:c.316A>C	NP_149355.1:p.Ile106Leu