Canonical Allele Identifier: CA470996015

Gene: FGF8

Linked Data

• MyVariant Identifiers: chr10:g.103531231G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771474G>A , CM000672.2:g.101771474G>A	GRCh38
NC_000010.10:g.103531231G>A , CM000672.1:g.103531231G>A	GRCh37
NC_000010.9:g.103521221G>A	NCBI36
NG_007151.1:g.9597C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.433C>T MANE Select	ENSP00000321797.2:p.Leu145=
ENST00000618991.5:c.121C>T	ENSP00000484420.1:p.Leu41=
ENST00000344255.8:c.400C>T	ENSP00000340039.3:p.Leu134=
ENST00000320185.6:c.433C>T	ENSP00000321797.2:p.Leu145=
ENST00000344255.7:c.400C>T	ENSP00000340039.3:p.Leu134=
ENST00000346714.7:c.313C>T	ENSP00000344306.3:p.Leu105=
ENST00000347978.2:c.346C>T	ENSP00000321945.2:p.Leu116=
ENST00000469792.6:c.*397C>T	ENSP00000473299.1:n.*397C>T
ENST00000485728.1:n.309C>T
ENST00000618991.4:c.121C>T	ENSP00000484420.1:p.Leu41=
NM_001206389.1:c.121C>T	NP_001193318.1:p.Leu41=
NM_006119.4:c.346C>T	NP_006110.1:p.Leu116=
NM_033163.3:c.433C>T	NP_149353.1:p.Leu145=
NM_033164.3:c.400C>T	NP_149354.1:p.Leu134=
NM_033165.3:c.313C>T	NP_149355.1:p.Leu105=
XM_011539509.1:c.355C>T	XP_011537811.1:p.Leu119=
XR_946251.1:n.278-23G>A
XR_946252.1:n.209-23G>A
XR_946253.1:n.207-23G>A
XR_946252.2:n.299-23G>A
XR_946253.2:n.297-23G>A
NM_006119.5:c.346C>T	NP_006110.1:p.Leu116=
NM_033163.4:c.433C>T	NP_149353.1:p.Leu145=
NM_033164.4:c.400C>T	NP_149354.1:p.Leu134=
NM_033165.4:c.313C>T	NP_149355.1:p.Leu105=
NM_001206389.2:c.121C>T	NP_001193318.1:p.Leu41=
NM_006119.6:c.346C>T	NP_006110.1:p.Leu116=
NM_033163.5:c.433C>T MANE Select	NP_149353.1:p.Leu145=
NM_033165.5:c.313C>T	NP_149355.1:p.Leu105=