Canonical Allele Identifier: CA470996274

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534493G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774736G>C , CM000672.2:g.101774736G>C	GRCh38
NC_000010.10:g.103534493G>C , CM000672.1:g.103534493G>C	GRCh37
NC_000010.9:g.103524483G>C	NCBI36
NG_007151.1:g.6335C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.333C>G MANE Select	ENSP00000321797.2:p.Pro111=
ENST00000618991.5:c.21C>G	ENSP00000484420.1:p.Pro7=
ENST00000344255.8:c.300C>G	ENSP00000340039.3:p.Pro100=
ENST00000320185.6:c.333C>G	ENSP00000321797.2:p.Pro111=
ENST00000344255.7:c.300C>G	ENSP00000340039.3:p.Pro100=
ENST00000346714.7:c.213C>G	ENSP00000344306.3:p.Pro71=
ENST00000347978.2:c.246C>G	ENSP00000321945.2:p.Pro82=
ENST00000469792.6:c.*297C>G	ENSP00000473299.1:n.*297C>G
ENST00000485728.1:n.209C>G
ENST00000618991.4:c.21C>G	ENSP00000484420.1:p.Pro7=
NM_001206389.1:c.21C>G	NP_001193318.1:p.Pro7=
NM_006119.4:c.246C>G	NP_006110.1:p.Pro82=
NM_033163.3:c.333C>G	NP_149353.1:p.Pro111=
NM_033164.3:c.300C>G	NP_149354.1:p.Pro100=
NM_033165.3:c.213C>G	NP_149355.1:p.Pro71=
XM_011539509.1:c.255C>G	XP_011537811.1:p.Pro85=
NM_006119.5:c.246C>G	NP_006110.1:p.Pro82=
NM_033163.4:c.333C>G	NP_149353.1:p.Pro111=
NM_033164.4:c.300C>G	NP_149354.1:p.Pro100=
NM_033165.4:c.213C>G	NP_149355.1:p.Pro71=
NM_001206389.2:c.21C>G	NP_001193318.1:p.Pro7=
NM_006119.6:c.246C>G	NP_006110.1:p.Pro82=
NM_033163.5:c.333C>G MANE Select	NP_149353.1:p.Pro111=
NM_033165.5:c.213C>G	NP_149355.1:p.Pro71=