Canonical Allele Identifier: CA377836625

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534556G>C (hg19) ; chr10:g.101774799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774799G>C , CM000672.2:g.101774799G>C	GRCh38
NC_000010.10:g.103534556G>C , CM000672.1:g.103534556G>C	GRCh37
NC_000010.9:g.103524546G>C	NCBI36
NG_007151.1:g.6272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.270C>G MANE Select	ENSP00000321797.2:p.Ser90Arg
ENST00000618991.5:c.-43C>G	ENSP00000484420.1:n.-43C>G
ENST00000344255.8:c.237C>G	ENSP00000340039.3:p.Ser79Arg
ENST00000320185.6:c.270C>G	ENSP00000321797.2:p.Ser90Arg
ENST00000344255.7:c.237C>G	ENSP00000340039.3:p.Ser79Arg
ENST00000346714.7:c.150C>G	ENSP00000344306.3:p.Ser50Arg
ENST00000347978.2:c.183C>G	ENSP00000321945.2:p.Ser61Arg
ENST00000469792.6:c.*234C>G	ENSP00000473299.1:n.*234C>G
ENST00000485728.1:n.146C>G
ENST00000618991.4:c.-43C>G	ENSP00000484420.1:n.-43C>G
NM_001206389.1:c.-43C>G	NP_001193318.1:n.-43C>G
NM_006119.4:c.183C>G	NP_006110.1:p.Ser61Arg
NM_033163.3:c.270C>G	NP_149353.1:p.Ser90Arg
NM_033164.3:c.237C>G	NP_149354.1:p.Ser79Arg
NM_033165.3:c.150C>G	NP_149355.1:p.Ser50Arg
XM_011539509.1:c.192C>G	XP_011537811.1:p.Ser64Arg
NM_006119.5:c.183C>G	NP_006110.1:p.Ser61Arg
NM_033163.4:c.270C>G	NP_149353.1:p.Ser90Arg
NM_033164.4:c.237C>G	NP_149354.1:p.Ser79Arg
NM_033165.4:c.150C>G	NP_149355.1:p.Ser50Arg
NM_001206389.2:c.-43C>G	NP_001193318.1:n.-43C>G
NM_006119.6:c.183C>G	NP_006110.1:p.Ser61Arg
NM_033163.5:c.270C>G MANE Select	NP_149353.1:p.Ser90Arg
NM_033165.5:c.150C>G	NP_149355.1:p.Ser50Arg