Canonical Allele Identifier: CA470996487

Gene: FGF8

Linked Data

• gnomAD v4: 10-101775208-C-CAGCGCA
• MyVariant Identifiers: chr10:g.103534965_103534966insAGCGCA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775208_101775209insAGCGCA , CM000672.2:g.101775208_101775209insAGCGCA	GRCh38
NC_000010.10:g.103534965_103534966insAGCGCA , CM000672.1:g.103534965_103534966insAGCGCA	GRCh37
NC_000010.9:g.103524955_103524956insAGCGCA	NCBI36
NG_007151.1:g.5862_5863insTGCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.77_78insTGCGCT MANE Select	ENSP00000321797.2:p.Pro26_Gly27insAlaLeu
ENST00000618991.5:c.-123-330_-123-329insTGCGCT	ENSP00000484420.1:n.-123-330_-123-329insTGCGCT
ENST00000344255.8:c.77_78insTGCGCT	ENSP00000340039.3:p.Pro26_Gly27insAlaLeu
ENST00000320185.6:c.77_78insTGCGCT	ENSP00000321797.2:p.Pro26_Gly27insAlaLeu
ENST00000344255.7:c.77_78insTGCGCT	ENSP00000340039.3:p.Pro26_Gly27insAlaLeu
ENST00000346714.7:c.70-330_70-329insTGCGCT	ENSP00000344306.3:n.70-330_70-329insTGCGCT
ENST00000347978.2:c.70-297_70-296insTGCGCT	ENSP00000321945.2:n.70-297_70-296insTGCGCT
ENST00000469792.6:c.*154-330_*154-329insTGCGCT	ENSP00000473299.1:n.*154-330_*154-329insTGCGCT
ENST00000485728.1:n.33-297_33-296insTGCGCT
ENST00000618991.4:c.-123-330_-123-329insTGCGCT	ENSP00000484420.1:n.-123-330_-123-329insTGCGCT
NM_001206389.1:c.-123-330_-123-329insTGCGCT	NP_001193318.1:n.-123-330_-123-329insTGCGCT
NM_006119.4:c.70-297_70-296insTGCGCT	NP_006110.1:n.70-297_70-296insTGCGCT
NM_033163.3:c.77_78insTGCGCT	NP_149353.1:p.Pro26_Gly27insAlaLeu
NM_033164.3:c.77_78insTGCGCT	NP_149354.1:p.Pro26_Gly27insAlaLeu
NM_033165.3:c.70-330_70-329insTGCGCT	NP_149355.1:n.70-330_70-329insTGCGCT
XM_011539509.1:c.79-297_79-296insTGCGCT	XP_011537811.1:n.79-297_79-296insTGCGCT
NM_006119.5:c.70-297_70-296insTGCGCT	NP_006110.1:n.70-297_70-296insTGCGCT
NM_033163.4:c.77_78insTGCGCT	NP_149353.1:p.Pro26_Gly27insAlaLeu
NM_033164.4:c.77_78insTGCGCT	NP_149354.1:p.Pro26_Gly27insAlaLeu
NM_033165.4:c.70-330_70-329insTGCGCT	NP_149355.1:n.70-330_70-329insTGCGCT
NM_001206389.2:c.-123-330_-123-329insTGCGCT	NP_001193318.1:n.-123-330_-123-329insTGCGCT
NM_006119.6:c.70-297_70-296insTGCGCT	NP_006110.1:n.70-297_70-296insTGCGCT
NM_033163.5:c.77_78insTGCGCT MANE Select	NP_149353.1:p.Pro26_Gly27insAlaLeu
NM_033165.5:c.70-330_70-329insTGCGCT	NP_149355.1:n.70-330_70-329insTGCGCT