Canonical Allele Identifier: CA1767395827
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992918_16992919delinsGT , CM000670.2:g.16992918_16992919delinsGT GRCh38
NC_000008.10:g.16850427_16850428delinsGT , CM000670.1:g.16850427_16850428delinsGT GRCh37
NC_000008.9:g.16894798_16894799delinsGT NCBI36
NG_015978.1:g.14247_14248delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*153_*154delinsAC MANE Select ENSP00000180166.5:n.*153_*154delinsAC
ENST00000180166.5:c.*153_*154delinsAC ENSP00000180166.5:n.*153_*154delinsAC
NM_019851.2:c.*153_*154delinsAC NP_062825.1:n.*153_*154delinsAC
NM_019851.3:c.*153_*154delinsAC MANE Select NP_062825.1:n.*153_*154delinsAC
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