Canonical Allele Identifier: CA2610619611

Gene: FGF8

Linked Data

• gnomAD v4: 10-101771317-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771317A>C , CM000672.2:g.101771317A>C	GRCh38
NC_000010.10:g.103531074A>C , CM000672.1:g.103531074A>C	GRCh37
NC_000010.9:g.103521064A>C	NCBI36
NG_007151.1:g.9754T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.444+146T>G MANE Select	ENSP00000321797.2:n.444+146T>G
ENST00000618991.5:c.132+146T>G	ENSP00000484420.1:n.132+146T>G
ENST00000344255.8:c.411+146T>G	ENSP00000340039.3:n.411+146T>G
ENST00000320185.6:c.444+146T>G	ENSP00000321797.2:n.444+146T>G
ENST00000344255.7:c.411+146T>G	ENSP00000340039.3:n.411+146T>G
ENST00000346714.7:c.324+146T>G	ENSP00000344306.3:n.324+146T>G
ENST00000347978.2:c.357+146T>G	ENSP00000321945.2:n.357+146T>G
ENST00000469792.6:c.*408+146T>G	ENSP00000473299.1:n.*408+146T>G
ENST00000485728.1:n.320+146T>G
ENST00000618991.4:c.132+146T>G	ENSP00000484420.1:n.132+146T>G
NM_001206389.1:c.132+146T>G	NP_001193318.1:n.132+146T>G
NM_006119.4:c.357+146T>G	NP_006110.1:n.357+146T>G
NM_033163.3:c.444+146T>G	NP_149353.1:n.444+146T>G
NM_033164.3:c.411+146T>G	NP_149354.1:n.411+146T>G
NM_033165.3:c.324+146T>G	NP_149355.1:n.324+146T>G
XM_011539509.1:c.366+146T>G	XP_011537811.1:n.366+146T>G
XR_946251.1:n.278-180A>C
XR_946252.1:n.209-180A>C
XR_946253.1:n.207-180A>C
XR_946252.2:n.299-180A>C
XR_946253.2:n.297-180A>C
NM_006119.5:c.357+146T>G	NP_006110.1:n.357+146T>G
NM_033163.4:c.444+146T>G	NP_149353.1:n.444+146T>G
NM_033164.4:c.411+146T>G	NP_149354.1:n.411+146T>G
NM_033165.4:c.324+146T>G	NP_149355.1:n.324+146T>G
NM_001206389.2:c.132+146T>G	NP_001193318.1:n.132+146T>G
NM_006119.6:c.357+146T>G	NP_006110.1:n.357+146T>G
NM_033163.5:c.444+146T>G MANE Select	NP_149353.1:n.444+146T>G
NM_033165.5:c.324+146T>G	NP_149355.1:n.324+146T>G