Canonical Allele Identifier: CA1879991518
Gene: FPGS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127800261_127800263delinsCAG , CM000671.2:g.127800261_127800263delinsCAG GRCh38
NC_000009.11:g.130562540_130562542delinsCAG , CM000671.1:g.130562540_130562542delinsCAG GRCh37
NC_000009.10:g.129602361_129602363delinsCAG NCBI36
NG_023245.1:g.2387_2389delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000479147.6:n.217-4024_217-4022delinsCAG
ENST00000479375.6:n.132-4024_132-4022delinsCAG
Search 100 bp 5'
Search 100 bp 3'