Canonical Allele Identifier: CA470996005

Gene: FGF8

Linked Data

• gnomAD v4: 10-101771463-C-T
• MyVariant Identifiers: chr10:g.103531220C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771463C>T , CM000672.2:g.101771463C>T	GRCh38
NC_000010.10:g.103531220C>T , CM000672.1:g.103531220C>T	GRCh37
NC_000010.9:g.103521210C>T	NCBI36
NG_007151.1:g.9608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.444G>A MANE Select	ENSP00000321797.2:p.Lys148=
ENST00000618991.5:c.132G>A	ENSP00000484420.1:p.Lys44=
ENST00000344255.8:c.411G>A	ENSP00000340039.3:p.Lys137=
ENST00000320185.6:c.444G>A	ENSP00000321797.2:p.Lys148=
ENST00000344255.7:c.411G>A	ENSP00000340039.3:p.Lys137=
ENST00000346714.7:c.324G>A	ENSP00000344306.3:p.Lys108=
ENST00000347978.2:c.357G>A	ENSP00000321945.2:p.Lys119=
ENST00000469792.6:c.*408G>A	ENSP00000473299.1:n.*408G>A
ENST00000485728.1:n.320G>A
ENST00000618991.4:c.132G>A	ENSP00000484420.1:p.Lys44=
NM_001206389.1:c.132G>A	NP_001193318.1:p.Lys44=
NM_006119.4:c.357G>A	NP_006110.1:p.Lys119=
NM_033163.3:c.444G>A	NP_149353.1:p.Lys148=
NM_033164.3:c.411G>A	NP_149354.1:p.Lys137=
NM_033165.3:c.324G>A	NP_149355.1:p.Lys108=
XM_011539509.1:c.366G>A	XP_011537811.1:p.Lys122=
XR_946251.1:n.278-34C>T
XR_946252.1:n.209-34C>T
XR_946253.1:n.207-34C>T
XR_946252.2:n.299-34C>T
XR_946253.2:n.297-34C>T
NM_006119.5:c.357G>A	NP_006110.1:p.Lys119=
NM_033163.4:c.444G>A	NP_149353.1:p.Lys148=
NM_033164.4:c.411G>A	NP_149354.1:p.Lys137=
NM_033165.4:c.324G>A	NP_149355.1:p.Lys108=
NM_001206389.2:c.132G>A	NP_001193318.1:p.Lys44=
NM_006119.6:c.357G>A	NP_006110.1:p.Lys119=
NM_033163.5:c.444G>A MANE Select	NP_149353.1:p.Lys148=
NM_033165.5:c.324G>A	NP_149355.1:p.Lys108=