Canonical Allele Identifier: CA2610620463

Gene: FGF8

Linked Data

• gnomAD v4: 10-101774978-C-CCCCTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774981_101774982insTGGCCC , CM000672.2:g.101774981_101774982insTGGCCC	GRCh38
NC_000010.10:g.103534738_103534739insTGGCCC , CM000672.1:g.103534738_103534739insTGGCCC	GRCh37
NC_000010.9:g.103524728_103524729insTGGCCC	NCBI36
NG_007151.1:g.6092_6093insCCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.157-67_157-66insCCAGGG MANE Select	ENSP00000321797.2:n.157-67_157-66insCCAGGG
ENST00000618991.5:c.-123-100_-123-99insCCAGGG	ENSP00000484420.1:n.-123-100_-123-99insCCAGGG
ENST00000344255.8:c.157-100_157-99insCCAGGG	ENSP00000340039.3:n.157-100_157-99insCCAGGG
ENST00000320185.6:c.157-67_157-66insCCAGGG	ENSP00000321797.2:n.157-67_157-66insCCAGGG
ENST00000344255.7:c.157-100_157-99insCCAGGG	ENSP00000340039.3:n.157-100_157-99insCCAGGG
ENST00000346714.7:c.70-100_70-99insCCAGGG	ENSP00000344306.3:n.70-100_70-99insCCAGGG
ENST00000347978.2:c.70-67_70-66insCCAGGG	ENSP00000321945.2:n.70-67_70-66insCCAGGG
ENST00000469792.6:c.*154-100_*154-99insCCAGGG	ENSP00000473299.1:n.*154-100_*154-99insCCAGGG
ENST00000485728.1:n.33-67_33-66insCCAGGG
ENST00000618991.4:c.-123-100_-123-99insCCAGGG	ENSP00000484420.1:n.-123-100_-123-99insCCAGGG
NM_001206389.1:c.-123-100_-123-99insCCAGGG	NP_001193318.1:n.-123-100_-123-99insCCAGGG
NM_006119.4:c.70-67_70-66insCCAGGG	NP_006110.1:n.70-67_70-66insCCAGGG
NM_033163.3:c.157-67_157-66insCCAGGG	NP_149353.1:n.157-67_157-66insCCAGGG
NM_033164.3:c.157-100_157-99insCCAGGG	NP_149354.1:n.157-100_157-99insCCAGGG
NM_033165.3:c.70-100_70-99insCCAGGG	NP_149355.1:n.70-100_70-99insCCAGGG
XM_011539509.1:c.79-67_79-66insCCAGGG	XP_011537811.1:n.79-67_79-66insCCAGGG
NM_006119.5:c.70-67_70-66insCCAGGG	NP_006110.1:n.70-67_70-66insCCAGGG
NM_033163.4:c.157-67_157-66insCCAGGG	NP_149353.1:n.157-67_157-66insCCAGGG
NM_033164.4:c.157-100_157-99insCCAGGG	NP_149354.1:n.157-100_157-99insCCAGGG
NM_033165.4:c.70-100_70-99insCCAGGG	NP_149355.1:n.70-100_70-99insCCAGGG
NM_001206389.2:c.-123-100_-123-99insCCAGGG	NP_001193318.1:n.-123-100_-123-99insCCAGGG
NM_006119.6:c.70-67_70-66insCCAGGG	NP_006110.1:n.70-67_70-66insCCAGGG
NM_033163.5:c.157-67_157-66insCCAGGG MANE Select	NP_149353.1:n.157-67_157-66insCCAGGG
NM_033165.5:c.70-100_70-99insCCAGGG	NP_149355.1:n.70-100_70-99insCCAGGG