Canonical Allele Identifier: CA377836230

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774755-A-G
• MyVariant Identifiers: chr10:g.103534512A>G (hg19) ; chr10:g.101774755A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774755A>G , CM000672.2:g.101774755A>G	GRCh38
NC_000010.10:g.103534512A>G , CM000672.1:g.103534512A>G	GRCh37
NC_000010.9:g.103524502A>G	NCBI36
NG_007151.1:g.6316T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.314T>C MANE Select	ENSP00000321797.2:p.Met105Thr
ENST00000618991.5:c.2T>C	ENSP00000484420.1:p.Met1Thr
ENST00000344255.8:c.281T>C	ENSP00000340039.3:p.Met94Thr
ENST00000320185.6:c.314T>C	ENSP00000321797.2:p.Met105Thr
ENST00000344255.7:c.281T>C	ENSP00000340039.3:p.Met94Thr
ENST00000346714.7:c.194T>C	ENSP00000344306.3:p.Met65Thr
ENST00000347978.2:c.227T>C	ENSP00000321945.2:p.Met76Thr
ENST00000469792.6:c.*278T>C	ENSP00000473299.1:n.*278T>C
ENST00000485728.1:n.190T>C
ENST00000618991.4:c.2T>C	ENSP00000484420.1:p.Met1Thr
NM_001206389.1:c.2T>C	NP_001193318.1:p.Met1Thr
NM_006119.4:c.227T>C	NP_006110.1:p.Met76Thr
NM_033163.3:c.314T>C	NP_149353.1:p.Met105Thr
NM_033164.3:c.281T>C	NP_149354.1:p.Met94Thr
NM_033165.3:c.194T>C	NP_149355.1:p.Met65Thr
XM_011539509.1:c.236T>C	XP_011537811.1:p.Met79Thr
NM_006119.5:c.227T>C	NP_006110.1:p.Met76Thr
NM_033163.4:c.314T>C	NP_149353.1:p.Met105Thr
NM_033164.4:c.281T>C	NP_149354.1:p.Met94Thr
NM_033165.4:c.194T>C	NP_149355.1:p.Met65Thr
NM_001206389.2:c.2T>C	NP_001193318.1:p.Met1Thr
NM_006119.6:c.227T>C	NP_006110.1:p.Met76Thr
NM_033163.5:c.314T>C MANE Select	NP_149353.1:p.Met105Thr
NM_033165.5:c.194T>C	NP_149355.1:p.Met65Thr