Canonical Allele Identifier: CA2779224013
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992928_16992929del , CM000670.2:g.16992928_16992929del GRCh38
NC_000008.10:g.16850437_16850438del , CM000670.1:g.16850437_16850438del GRCh37
NC_000008.9:g.16894808_16894809del NCBI36
NG_015978.1:g.14239_14240del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*145_*146del MANE Select ENSP00000180166.5:n.*145_*146del
ENST00000180166.5:c.*145_*146del ENSP00000180166.5:n.*145_*146del
NM_019851.2:c.*145_*146del NP_062825.1:n.*145_*146del
NM_019851.3:c.*145_*146del MANE Select NP_062825.1:n.*145_*146del