Canonical Allele Identifier: CA1767395891

Gene: FGF20

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992990_16993003delinsCTTGGGTCATTATT , CM000670.2:g.16992990_16993003delinsCTTGGGTCATTATT	GRCh38
NC_000008.10:g.16850499_16850512delinsCTTGGGTCATTATT , CM000670.1:g.16850499_16850512delinsCTTGGGTCATTATT	GRCh37
NC_000008.9:g.16894870_16894883delinsCTTGGGTCATTATT	NCBI36
NG_015978.1:g.14163_14176delinsAATAATGACCCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*69_*82delinsAATAATGACCCAAG MANE Select	ENSP00000180166.5:n.*69_*82delinsAATAATGACCCAAG
ENST00000180166.5:c.*69_*82delinsAATAATGACCCAAG	ENSP00000180166.5:n.*69_*82delinsAATAATGACCCAAG
ENST00000519941.1:c.409_422delinsAATAATGACCCAAG
NM_019851.2:c.*69_*82delinsAATAATGACCCAAG	NP_062825.1:n.*69_*82delinsAATAATGACCCAAG
NM_019851.3:c.*69_*82delinsAATAATGACCCAAG MANE Select	NP_062825.1:n.*69_*82delinsAATAATGACCCAAG