Canonical Allele Identifier: CA377836629

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534557C>A (hg19) ; chr10:g.101774800C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774800C>A , CM000672.2:g.101774800C>A	GRCh38
NC_000010.10:g.103534557C>A , CM000672.1:g.103534557C>A	GRCh37
NC_000010.9:g.103524547C>A	NCBI36
NG_007151.1:g.6271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.269G>T MANE Select	ENSP00000321797.2:p.Ser90Ile
ENST00000618991.5:c.-44G>T	ENSP00000484420.1:n.-44G>T
ENST00000344255.8:c.236G>T	ENSP00000340039.3:p.Ser79Ile
ENST00000320185.6:c.269G>T	ENSP00000321797.2:p.Ser90Ile
ENST00000344255.7:c.236G>T	ENSP00000340039.3:p.Ser79Ile
ENST00000346714.7:c.149G>T	ENSP00000344306.3:p.Ser50Ile
ENST00000347978.2:c.182G>T	ENSP00000321945.2:p.Ser61Ile
ENST00000469792.6:c.*233G>T	ENSP00000473299.1:n.*233G>T
ENST00000485728.1:n.145G>T
ENST00000618991.4:c.-44G>T	ENSP00000484420.1:n.-44G>T
NM_001206389.1:c.-44G>T	NP_001193318.1:n.-44G>T
NM_006119.4:c.182G>T	NP_006110.1:p.Ser61Ile
NM_033163.3:c.269G>T	NP_149353.1:p.Ser90Ile
NM_033164.3:c.236G>T	NP_149354.1:p.Ser79Ile
NM_033165.3:c.149G>T	NP_149355.1:p.Ser50Ile
XM_011539509.1:c.191G>T	XP_011537811.1:p.Ser64Ile
NM_006119.5:c.182G>T	NP_006110.1:p.Ser61Ile
NM_033163.4:c.269G>T	NP_149353.1:p.Ser90Ile
NM_033164.4:c.236G>T	NP_149354.1:p.Ser79Ile
NM_033165.4:c.149G>T	NP_149355.1:p.Ser50Ile
NM_001206389.2:c.-44G>T	NP_001193318.1:n.-44G>T
NM_006119.6:c.182G>T	NP_006110.1:p.Ser61Ile
NM_033163.5:c.269G>T MANE Select	NP_149353.1:p.Ser90Ile
NM_033165.5:c.149G>T	NP_149355.1:p.Ser50Ile