Canonical Allele Identifier: CA1932372867

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771738_101771739delinsTG , CM000672.2:g.101771738_101771739delinsTG	GRCh38
NC_000010.10:g.103531495_103531496delinsTG , CM000672.1:g.103531495_103531496delinsTG	GRCh37
NC_000010.9:g.103521485_103521486delinsTG	NCBI36
NG_007151.1:g.9332_9333delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.338-170_338-169delinsCA MANE Select	ENSP00000321797.2:n.338-170_338-169delinsCA
ENST00000618991.5:c.26-170_26-169delinsCA	ENSP00000484420.1:n.26-170_26-169delinsCA
ENST00000344255.8:c.305-170_305-169delinsCA	ENSP00000340039.3:n.305-170_305-169delinsCA
ENST00000320185.6:c.338-170_338-169delinsCA	ENSP00000321797.2:n.338-170_338-169delinsCA
ENST00000344255.7:c.305-170_305-169delinsCA	ENSP00000340039.3:n.305-170_305-169delinsCA
ENST00000346714.7:c.218-170_218-169delinsCA	ENSP00000344306.3:n.218-170_218-169delinsCA
ENST00000347978.2:c.251-170_251-169delinsCA	ENSP00000321945.2:n.251-170_251-169delinsCA
ENST00000469792.6:c.*302-170_*302-169delinsCA	ENSP00000473299.1:n.*302-170_*302-169delinsCA
ENST00000485728.1:n.214-170_214-169delinsCA
ENST00000618991.4:c.26-170_26-169delinsCA	ENSP00000484420.1:n.26-170_26-169delinsCA
NM_001206389.1:c.26-170_26-169delinsCA	NP_001193318.1:n.26-170_26-169delinsCA
NM_006119.4:c.251-170_251-169delinsCA	NP_006110.1:n.251-170_251-169delinsCA
NM_033163.3:c.338-170_338-169delinsCA	NP_149353.1:n.338-170_338-169delinsCA
NM_033164.3:c.305-170_305-169delinsCA	NP_149354.1:n.305-170_305-169delinsCA
NM_033165.3:c.218-170_218-169delinsCA	NP_149355.1:n.218-170_218-169delinsCA
XM_011539509.1:c.260-170_260-169delinsCA	XP_011537811.1:n.260-170_260-169delinsCA
XR_946252.2:n.540_541delinsTG
XR_946253.2:n.538_539delinsTG
NM_006119.5:c.251-170_251-169delinsCA	NP_006110.1:n.251-170_251-169delinsCA
NM_033163.4:c.338-170_338-169delinsCA	NP_149353.1:n.338-170_338-169delinsCA
NM_033164.4:c.305-170_305-169delinsCA	NP_149354.1:n.305-170_305-169delinsCA
NM_033165.4:c.218-170_218-169delinsCA	NP_149355.1:n.218-170_218-169delinsCA
NM_001206389.2:c.26-170_26-169delinsCA	NP_001193318.1:n.26-170_26-169delinsCA
NM_006119.6:c.251-170_251-169delinsCA	NP_006110.1:n.251-170_251-169delinsCA
NM_033163.5:c.338-170_338-169delinsCA MANE Select	NP_149353.1:n.338-170_338-169delinsCA
NM_033165.5:c.218-170_218-169delinsCA	NP_149355.1:n.218-170_218-169delinsCA