Canonical Allele Identifier: CA377836099

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774738-G-T
• MyVariant Identifiers: chr10:g.103534495G>T (hg19) ; chr10:g.101774738G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774738G>T , CM000672.2:g.101774738G>T	GRCh38
NC_000010.10:g.103534495G>T , CM000672.1:g.103534495G>T	GRCh37
NC_000010.9:g.103524485G>T	NCBI36
NG_007151.1:g.6333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.331C>A MANE Select	ENSP00000321797.2:p.Pro111Thr
ENST00000618991.5:c.19C>A	ENSP00000484420.1:p.Pro7Thr
ENST00000344255.8:c.298C>A	ENSP00000340039.3:p.Pro100Thr
ENST00000320185.6:c.331C>A	ENSP00000321797.2:p.Pro111Thr
ENST00000344255.7:c.298C>A	ENSP00000340039.3:p.Pro100Thr
ENST00000346714.7:c.211C>A	ENSP00000344306.3:p.Pro71Thr
ENST00000347978.2:c.244C>A	ENSP00000321945.2:p.Pro82Thr
ENST00000469792.6:c.*295C>A	ENSP00000473299.1:n.*295C>A
ENST00000485728.1:n.207C>A
ENST00000618991.4:c.19C>A	ENSP00000484420.1:p.Pro7Thr
NM_001206389.1:c.19C>A	NP_001193318.1:p.Pro7Thr
NM_006119.4:c.244C>A	NP_006110.1:p.Pro82Thr
NM_033163.3:c.331C>A	NP_149353.1:p.Pro111Thr
NM_033164.3:c.298C>A	NP_149354.1:p.Pro100Thr
NM_033165.3:c.211C>A	NP_149355.1:p.Pro71Thr
XM_011539509.1:c.253C>A	XP_011537811.1:p.Pro85Thr
NM_006119.5:c.244C>A	NP_006110.1:p.Pro82Thr
NM_033163.4:c.331C>A	NP_149353.1:p.Pro111Thr
NM_033164.4:c.298C>A	NP_149354.1:p.Pro100Thr
NM_033165.4:c.211C>A	NP_149355.1:p.Pro71Thr
NM_001206389.2:c.19C>A	NP_001193318.1:p.Pro7Thr
NM_006119.6:c.244C>A	NP_006110.1:p.Pro82Thr
NM_033163.5:c.331C>A MANE Select	NP_149353.1:p.Pro111Thr
NM_033165.5:c.211C>A	NP_149355.1:p.Pro71Thr