Canonical Allele Identifier: CA1879991859
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800458_127800460delinsTCC , CM000671.2:g.127800458_127800460delinsTCC GRCh38
NC_000009.11:g.130562737_130562739delinsTCC , CM000671.1:g.130562737_130562739delinsTCC GRCh37
NC_000009.10:g.129602558_129602560delinsTCC NCBI36
NG_023245.1:g.2584_2586delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3827_217-3825delinsTCC
ENST00000479375.6:n.132-3827_132-3825delinsTCC