Canonical Allele Identifier: CA1932377098

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775082_101775093delinsGCAGACCCAGCC , CM000672.2:g.101775082_101775093delinsGCAGACCCAGCC	GRCh38
NC_000010.10:g.103534839_103534850delinsGCAGACCCAGCC , CM000672.1:g.103534839_103534850delinsGCAGACCCAGCC	GRCh37
NC_000010.9:g.103524829_103524840delinsGCAGACCCAGCC	NCBI36
NG_007151.1:g.5978_5989delinsGGCTGGGTCTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.156+37_156+48delinsGGCTGGGTCTGC MANE Select	ENSP00000321797.2:n.156+37_156+48delinsGG...
ENST00000618991.5:c.-123-214_-123-203delinsGGCTGGGTCTGC	ENSP00000484420.1:n.-123-214_-123-203deli...
ENST00000344255.8:c.156+37_156+48delinsGGCTGGGTCTGC	ENSP00000340039.3:n.156+37_156+48delinsGG...
ENST00000320185.6:c.156+37_156+48delinsGGCTGGGTCTGC	ENSP00000321797.2:n.156+37_156+48delinsGG...
ENST00000344255.7:c.156+37_156+48delinsGGCTGGGTCTGC	ENSP00000340039.3:n.156+37_156+48delinsGG...
ENST00000346714.7:c.70-214_70-203delinsGGCTGGGTCTGC	ENSP00000344306.3:n.70-214_70-203delinsGG...
ENST00000347978.2:c.70-181_70-170delinsGGCTGGGTCTGC	ENSP00000321945.2:n.70-181_70-170delinsGG...
ENST00000469792.6:c.*154-214_*154-203delinsGGCTGGGTCTGC	ENSP00000473299.1:n.*154-214_*154-203deli...
ENST00000485728.1:n.33-181_33-170delinsGGCTGGGTCTGC
ENST00000618991.4:c.-123-214_-123-203delinsGGCTGGGTCTGC	ENSP00000484420.1:n.-123-214_-123-203deli...
NM_001206389.1:c.-123-214_-123-203delinsGGCTGGGTCTGC	NP_001193318.1:n.-123-214_-123-203delinsG...
NM_006119.4:c.70-181_70-170delinsGGCTGGGTCTGC	NP_006110.1:n.70-181_70-170delinsGGCTGGGT...
NM_033163.3:c.156+37_156+48delinsGGCTGGGTCTGC	NP_149353.1:n.156+37_156+48delinsGGCTGGGT...
NM_033164.3:c.156+37_156+48delinsGGCTGGGTCTGC	NP_149354.1:n.156+37_156+48delinsGGCTGGGT...
NM_033165.3:c.70-214_70-203delinsGGCTGGGTCTGC	NP_149355.1:n.70-214_70-203delinsGGCTGGGT...
XM_011539509.1:c.79-181_79-170delinsGGCTGGGTCTGC	XP_011537811.1:n.79-181_79-170delinsGGCTG...
NM_006119.5:c.70-181_70-170delinsGGCTGGGTCTGC	NP_006110.1:n.70-181_70-170delinsGGCTGGGT...
NM_033163.4:c.156+37_156+48delinsGGCTGGGTCTGC	NP_149353.1:n.156+37_156+48delinsGGCTGGGT...
NM_033164.4:c.156+37_156+48delinsGGCTGGGTCTGC	NP_149354.1:n.156+37_156+48delinsGGCTGGGT...
NM_033165.4:c.70-214_70-203delinsGGCTGGGTCTGC	NP_149355.1:n.70-214_70-203delinsGGCTGGGT...
NM_001206389.2:c.-123-214_-123-203delinsGGCTGGGTCTGC	NP_001193318.1:n.-123-214_-123-203delinsG...
NM_006119.6:c.70-181_70-170delinsGGCTGGGTCTGC	NP_006110.1:n.70-181_70-170delinsGGCTGGGT...
NM_033163.5:c.156+37_156+48delinsGGCTGGGTCTGC MANE Select	NP_149353.1:n.156+37_156+48delinsGGCTGGGT...
NM_033165.5:c.70-214_70-203delinsGGCTGGGTCTGC	NP_149355.1:n.70-214_70-203delinsGGCTGGGT...