Canonical Allele Identifier: CA377836631

Gene: FGF8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.269G>C MANE Select	ENSP00000321797.2:p.Ser90Thr
ENST00000618991.5:c.-44G>C	ENSP00000484420.1:n.-44G>C
ENST00000344255.8:c.236G>C	ENSP00000340039.3:p.Ser79Thr
ENST00000320185.6:c.269G>C	ENSP00000321797.2:p.Ser90Thr
ENST00000344255.7:c.236G>C	ENSP00000340039.3:p.Ser79Thr
ENST00000346714.7:c.149G>C	ENSP00000344306.3:p.Ser50Thr
ENST00000347978.2:c.182G>C	ENSP00000321945.2:p.Ser61Thr
ENST00000469792.6:c.*233G>C	ENSP00000473299.1:n.*233G>C
ENST00000485728.1:n.145G>C
ENST00000618991.4:c.-44G>C	ENSP00000484420.1:n.-44G>C
NM_001206389.1:c.-44G>C	NP_001193318.1:n.-44G>C
NM_006119.4:c.182G>C	NP_006110.1:p.Ser61Thr
NM_033163.3:c.269G>C	NP_149353.1:p.Ser90Thr
NM_033164.3:c.236G>C	NP_149354.1:p.Ser79Thr
NM_033165.3:c.149G>C	NP_149355.1:p.Ser50Thr
XM_011539509.1:c.191G>C	XP_011537811.1:p.Ser64Thr
NM_006119.5:c.182G>C	NP_006110.1:p.Ser61Thr
NM_033163.4:c.269G>C	NP_149353.1:p.Ser90Thr
NM_033164.4:c.236G>C	NP_149354.1:p.Ser79Thr
NM_033165.4:c.149G>C	NP_149355.1:p.Ser50Thr
NM_001206389.2:c.-44G>C	NP_001193318.1:n.-44G>C
NM_006119.6:c.182G>C	NP_006110.1:p.Ser61Thr
NM_033163.5:c.269G>C MANE Select	NP_149353.1:p.Ser90Thr
NM_033165.5:c.149G>C	NP_149355.1:p.Ser50Thr