Canonical Allele Identifier: CA470996029

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531253G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771496G>A , CM000672.2:g.101771496G>A	GRCh38
NC_000010.10:g.103531253G>A , CM000672.1:g.103531253G>A	GRCh37
NC_000010.9:g.103521243G>A	NCBI36
NG_007151.1:g.9575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.411C>T MANE Select	ENSP00000321797.2:p.Ile137=
ENST00000618991.5:c.99C>T	ENSP00000484420.1:p.Ile33=
ENST00000344255.8:c.378C>T	ENSP00000340039.3:p.Ile126=
ENST00000320185.6:c.411C>T	ENSP00000321797.2:p.Ile137=
ENST00000344255.7:c.378C>T	ENSP00000340039.3:p.Ile126=
ENST00000346714.7:c.291C>T	ENSP00000344306.3:p.Ile97=
ENST00000347978.2:c.324C>T	ENSP00000321945.2:p.Ile108=
ENST00000469792.6:c.*375C>T	ENSP00000473299.1:n.*375C>T
ENST00000485728.1:n.287C>T
ENST00000618991.4:c.99C>T	ENSP00000484420.1:p.Ile33=
NM_001206389.1:c.99C>T	NP_001193318.1:p.Ile33=
NM_006119.4:c.324C>T	NP_006110.1:p.Ile108=
NM_033163.3:c.411C>T	NP_149353.1:p.Ile137=
NM_033164.3:c.378C>T	NP_149354.1:p.Ile126=
NM_033165.3:c.291C>T	NP_149355.1:p.Ile97=
XM_011539509.1:c.333C>T	XP_011537811.1:p.Ile111=
XR_946251.1:n.278-1G>A
XR_946252.1:n.209-1G>A
XR_946253.1:n.207-1G>A
XR_946252.2:n.299-1G>A
XR_946253.2:n.297-1G>A
NM_006119.5:c.324C>T	NP_006110.1:p.Ile108=
NM_033163.4:c.411C>T	NP_149353.1:p.Ile137=
NM_033164.4:c.378C>T	NP_149354.1:p.Ile126=
NM_033165.4:c.291C>T	NP_149355.1:p.Ile97=
NM_001206389.2:c.99C>T	NP_001193318.1:p.Ile33=
NM_006119.6:c.324C>T	NP_006110.1:p.Ile108=
NM_033163.5:c.411C>T MANE Select	NP_149353.1:p.Ile137=
NM_033165.5:c.291C>T	NP_149355.1:p.Ile97=