Canonical Allele Identifier: CA2000616474
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226400_112226401delinsGC , CM000673.2:g.112226400_112226401delinsGC GRCh38
NC_000011.9:g.112097123_112097124delinsGC , CM000673.1:g.112097123_112097124delinsGC GRCh37
NC_000011.8:g.111602333_111602334delinsGC NCBI36
NG_008743.1:g.5036_5037delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.7:c.-44_-43delinsGC ENSP00000280362.3:n.-44_-43delinsGC
ENST00000525645.1:n.32_33delinsGC
ENST00000528679.5:c.-44_-43delinsGC ENSP00000435895.1:n.-44_-43delinsGC
ENST00000531673.5:c.-44_-43delinsGC ENSP00000433469.1:n.-44_-43delinsGC
NM_000317.2:c.-44_-43delinsGC NP_000308.1:n.-44_-43delinsGC