Canonical Allele Identifier: CA2572851168
Gene: PTS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228552_112228553insGC , CM000673.2:g.112228552_112228553insGC GRCh38
NC_000011.9:g.112099275_112099276insGC , CM000673.1:g.112099275_112099276insGC GRCh37
NC_000011.8:g.111604485_111604486insGC NCBI36
NG_008743.1:g.7188_7189insGC

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-42_84-41insGC MANE Select ENSP00000280362.3:n.84-42_84-41insGC
ENST00000280362.7:c.84-42_84-41insGC ENSP00000280362.3:n.84-42_84-41insGC
ENST00000524931.1:c.-121-42_-121-41insGC ENSP00000434688.1:n.-121-42_-121-41insGC
ENST00000525645.1:n.159-42_159-41insGC
ENST00000525803.1:c.84-42_84-41insGC ENSP00000431750.1:n.84-42_84-41insGC
ENST00000528679.5:c.84-42_84-41insGC ENSP00000435895.1:n.84-42_84-41insGC
ENST00000531673.5:c.84-42_84-41insGC ENSP00000433469.1:n.84-42_84-41insGC
NM_000317.2:c.84-42_84-41insGC NP_000308.1:n.84-42_84-41insGC
NM_000317.3:c.84-42_84-41insGC MANE Select NP_000308.1:n.84-42_84-41insGC
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