Canonical Allele Identifier: CA2574980261
Gene: PTS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228584T>G , CM000673.2:g.112228584T>G GRCh38
NC_000011.9:g.112099307T>G , CM000673.1:g.112099307T>G GRCh37
NC_000011.8:g.111604517T>G NCBI36
NG_008743.1:g.7220T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-10T>G MANE Select ENSP00000280362.3:n.84-10T>G
ENST00000280362.7:c.84-10T>G ENSP00000280362.3:n.84-10T>G
ENST00000524931.1:c.-121-10T>G ENSP00000434688.1:n.-121-10T>G
ENST00000525645.1:n.159-10T>G
ENST00000525803.1:c.84-10T>G ENSP00000431750.1:n.84-10T>G
ENST00000528679.5:c.84-10T>G ENSP00000435895.1:n.84-10T>G
ENST00000531673.5:c.84-10T>G ENSP00000433469.1:n.84-10T>G
NM_000317.2:c.84-10T>G NP_000308.1:n.84-10T>G
NM_000317.3:c.84-10T>G MANE Select NP_000308.1:n.84-10T>G
Search 100 bp 5'
Search 100 bp 3'