Canonical Allele Identifier: CA1767396057
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993088_16993094delinsAGGTCCT , CM000670.2:g.16993088_16993094delinsAGGTCCT GRCh38
NC_000008.10:g.16850597_16850603delinsAGGTCCT , CM000670.1:g.16850597_16850603delinsAGGTCCT GRCh37
NC_000008.9:g.16894968_16894974delinsAGGTCCT NCBI36
NG_015978.1:g.14072_14078delinsAGGACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.614_620delinsAGGACCT MANE Select ENSP00000180166.5:p.Lys205=
ENST00000180166.5:c.614_620delinsAGGACCT ENSP00000180166.5:p.Lys205=
ENST00000519941.1:c.318_324delinsAGGACCT
NM_019851.2:c.614_620delinsAGGACCT NP_062825.1:p.Lys205=
NM_019851.3:c.614_620delinsAGGACCT MANE Select NP_062825.1:p.Lys205=