Canonical Allele Identifier: CA1879991647
Gene: FPGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800327_127800329delinsTCA , CM000671.2:g.127800327_127800329delinsTCA GRCh38
NC_000009.11:g.130562606_130562608delinsTCA , CM000671.1:g.130562606_130562608delinsTCA GRCh37
NC_000009.10:g.129602427_129602429delinsTCA NCBI36
NG_023245.1:g.2453_2455delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-3958_217-3956delinsTCA
ENST00000479375.6:n.132-3958_132-3956delinsTCA