Canonical Allele Identifier: CA1932372920
Gene: FGF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101771753_101771754delinsAC , CM000672.2:g.101771753_101771754delinsAC GRCh38
NC_000010.10:g.103531510_103531511delinsAC , CM000672.1:g.103531510_103531511delinsAC GRCh37
NC_000010.9:g.103521500_103521501delinsAC NCBI36
NG_007151.1:g.9317_9318delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.338-185_338-184delinsGT MANE Select ENSP00000321797.2:n.338-185_338-184delinsGT
ENST00000618991.5:c.26-185_26-184delinsGT ENSP00000484420.1:n.26-185_26-184delinsGT
ENST00000344255.8:c.305-185_305-184delinsGT ENSP00000340039.3:n.305-185_305-184delinsGT
ENST00000320185.6:c.338-185_338-184delinsGT ENSP00000321797.2:n.338-185_338-184delinsGT
ENST00000344255.7:c.305-185_305-184delinsGT ENSP00000340039.3:n.305-185_305-184delinsGT
ENST00000346714.7:c.218-185_218-184delinsGT ENSP00000344306.3:n.218-185_218-184delinsGT
ENST00000347978.2:c.251-185_251-184delinsGT ENSP00000321945.2:n.251-185_251-184delinsGT
ENST00000469792.6:c.*302-185_*302-184delinsGT ENSP00000473299.1:n.*302-185_*302-184delinsGT
ENST00000485728.1:n.214-185_214-184delinsGT
ENST00000618991.4:c.26-185_26-184delinsGT ENSP00000484420.1:n.26-185_26-184delinsGT
NM_001206389.1:c.26-185_26-184delinsGT NP_001193318.1:n.26-185_26-184delinsGT
NM_006119.4:c.251-185_251-184delinsGT NP_006110.1:n.251-185_251-184delinsGT
NM_033163.3:c.338-185_338-184delinsGT NP_149353.1:n.338-185_338-184delinsGT
NM_033164.3:c.305-185_305-184delinsGT NP_149354.1:n.305-185_305-184delinsGT
NM_033165.3:c.218-185_218-184delinsGT NP_149355.1:n.218-185_218-184delinsGT
XM_011539509.1:c.260-185_260-184delinsGT XP_011537811.1:n.260-185_260-184delinsGT
XR_946252.2:n.555_556delinsAC
XR_946253.2:n.553_554delinsAC
NM_006119.5:c.251-185_251-184delinsGT NP_006110.1:n.251-185_251-184delinsGT
NM_033163.4:c.338-185_338-184delinsGT NP_149353.1:n.338-185_338-184delinsGT
NM_033164.4:c.305-185_305-184delinsGT NP_149354.1:n.305-185_305-184delinsGT
NM_033165.4:c.218-185_218-184delinsGT NP_149355.1:n.218-185_218-184delinsGT
NM_001206389.2:c.26-185_26-184delinsGT NP_001193318.1:n.26-185_26-184delinsGT
NM_006119.6:c.251-185_251-184delinsGT NP_006110.1:n.251-185_251-184delinsGT
NM_033163.5:c.338-185_338-184delinsGT MANE Select NP_149353.1:n.338-185_338-184delinsGT
NM_033165.5:c.218-185_218-184delinsGT NP_149355.1:n.218-185_218-184delinsGT