Canonical Allele Identifier: CA1767395896

Gene: FGF20

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992992_16992993delinsTG , CM000670.2:g.16992992_16992993delinsTG	GRCh38
NC_000008.10:g.16850501_16850502delinsTG , CM000670.1:g.16850501_16850502delinsTG	GRCh37
NC_000008.9:g.16894872_16894873delinsTG	NCBI36
NG_015978.1:g.14173_14174delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*79_*80delinsCA MANE Select	ENSP00000180166.5:n.*79_*80delinsCA
ENST00000180166.5:c.*79_*80delinsCA	ENSP00000180166.5:n.*79_*80delinsCA
ENST00000519941.1:c.419_420delinsCA
NM_019851.2:c.*79_*80delinsCA	NP_062825.1:n.*79_*80delinsCA
NM_019851.3:c.*79_*80delinsCA MANE Select	NP_062825.1:n.*79_*80delinsCA