Canonical Allele Identifier: CA377834481

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531293C>G (hg19) ; chr10:g.101771536C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771536C>G , CM000672.2:g.101771536C>G	GRCh38
NC_000010.10:g.103531293C>G , CM000672.1:g.103531293C>G	GRCh37
NC_000010.9:g.103521283C>G	NCBI36
NG_007151.1:g.9535G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.371G>C MANE Select	ENSP00000321797.2:p.Ser124Thr
ENST00000618991.5:c.59G>C	ENSP00000484420.1:p.Ser20Thr
ENST00000344255.8:c.338G>C	ENSP00000340039.3:p.Ser113Thr
ENST00000320185.6:c.371G>C	ENSP00000321797.2:p.Ser124Thr
ENST00000344255.7:c.338G>C	ENSP00000340039.3:p.Ser113Thr
ENST00000346714.7:c.251G>C	ENSP00000344306.3:p.Ser84Thr
ENST00000347978.2:c.284G>C	ENSP00000321945.2:p.Ser95Thr
ENST00000469792.6:c.*335G>C	ENSP00000473299.1:n.*335G>C
ENST00000485728.1:n.247G>C
ENST00000618991.4:c.59G>C	ENSP00000484420.1:p.Ser20Thr
NM_001206389.1:c.59G>C	NP_001193318.1:p.Ser20Thr
NM_006119.4:c.284G>C	NP_006110.1:p.Ser95Thr
NM_033163.3:c.371G>C	NP_149353.1:p.Ser124Thr
NM_033164.3:c.338G>C	NP_149354.1:p.Ser113Thr
NM_033165.3:c.251G>C	NP_149355.1:p.Ser84Thr
XM_011539509.1:c.293G>C	XP_011537811.1:p.Ser98Thr
XR_946251.1:n.317C>G
XR_946252.1:n.248C>G
XR_946253.1:n.246C>G
XR_946252.2:n.338C>G
XR_946253.2:n.336C>G
NM_006119.5:c.284G>C	NP_006110.1:p.Ser95Thr
NM_033163.4:c.371G>C	NP_149353.1:p.Ser124Thr
NM_033164.4:c.338G>C	NP_149354.1:p.Ser113Thr
NM_033165.4:c.251G>C	NP_149355.1:p.Ser84Thr
NM_001206389.2:c.59G>C	NP_001193318.1:p.Ser20Thr
NM_006119.6:c.284G>C	NP_006110.1:p.Ser95Thr
NM_033163.5:c.371G>C MANE Select	NP_149353.1:p.Ser124Thr
NM_033165.5:c.251G>C	NP_149355.1:p.Ser84Thr