Canonical Allele Identifier: CA377836225

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103534511C>G (hg19) ; chr10:g.101774754C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774754C>G , CM000672.2:g.101774754C>G	GRCh38
NC_000010.10:g.103534511C>G , CM000672.1:g.103534511C>G	GRCh37
NC_000010.9:g.103524501C>G	NCBI36
NG_007151.1:g.6317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.315G>C MANE Select	ENSP00000321797.2:p.Met105Ile
ENST00000618991.5:c.3G>C	ENSP00000484420.1:p.Met1Ile
ENST00000344255.8:c.282G>C	ENSP00000340039.3:p.Met94Ile
ENST00000320185.6:c.315G>C	ENSP00000321797.2:p.Met105Ile
ENST00000344255.7:c.282G>C	ENSP00000340039.3:p.Met94Ile
ENST00000346714.7:c.195G>C	ENSP00000344306.3:p.Met65Ile
ENST00000347978.2:c.228G>C	ENSP00000321945.2:p.Met76Ile
ENST00000469792.6:c.*279G>C	ENSP00000473299.1:n.*279G>C
ENST00000485728.1:n.191G>C
ENST00000618991.4:c.3G>C	ENSP00000484420.1:p.Met1Ile
NM_001206389.1:c.3G>C	NP_001193318.1:p.Met1Ile
NM_006119.4:c.228G>C	NP_006110.1:p.Met76Ile
NM_033163.3:c.315G>C	NP_149353.1:p.Met105Ile
NM_033164.3:c.282G>C	NP_149354.1:p.Met94Ile
NM_033165.3:c.195G>C	NP_149355.1:p.Met65Ile
XM_011539509.1:c.237G>C	XP_011537811.1:p.Met79Ile
NM_006119.5:c.228G>C	NP_006110.1:p.Met76Ile
NM_033163.4:c.315G>C	NP_149353.1:p.Met105Ile
NM_033164.4:c.282G>C	NP_149354.1:p.Met94Ile
NM_033165.4:c.195G>C	NP_149355.1:p.Met65Ile
NM_001206389.2:c.3G>C	NP_001193318.1:p.Met1Ile
NM_006119.6:c.228G>C	NP_006110.1:p.Met76Ile
NM_033163.5:c.315G>C MANE Select	NP_149353.1:p.Met105Ile
NM_033165.5:c.195G>C	NP_149355.1:p.Met65Ile