Canonical Allele Identifier: CA2000617568
Gene: PTS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228514A= , CM000673.2:g.112228514A= GRCh38
NC_000011.9:g.112099237A= , CM000673.1:g.112099237A= GRCh37
NC_000011.8:g.111604447A= NCBI36
NG_008743.1:g.7150A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.84-80A= MANE Select ENSP00000280362.3:n.84-80A=
ENST00000280362.7:c.84-80A= ENSP00000280362.3:n.84-80A=
ENST00000524931.1:c.-121-80A= ENSP00000434688.1:n.-121-80A=
ENST00000525645.1:n.159-80A=
ENST00000525803.1:c.84-80A= ENSP00000431750.1:n.84-80A=
ENST00000528679.5:c.84-80A= ENSP00000435895.1:n.84-80A=
ENST00000531673.5:c.84-80A= ENSP00000433469.1:n.84-80A=
NM_000317.2:c.84-80A= NP_000308.1:n.84-80A=
NM_000317.3:c.84-80A= MANE Select NP_000308.1:n.84-80A=
Search 100 bp 5'
Search 100 bp 3'