Canonical Allele Identifier: CA2615999727
Gene: PTS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228551T>C , CM000673.2:g.112228551T>C GRCh38
NC_000011.9:g.112099274T>C , CM000673.1:g.112099274T>C GRCh37
NC_000011.8:g.111604484T>C NCBI36
NG_008743.1:g.7187T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-43T>C MANE Select ENSP00000280362.3:n.84-43T>C
ENST00000280362.7:c.84-43T>C ENSP00000280362.3:n.84-43T>C
ENST00000524931.1:c.-121-43T>C ENSP00000434688.1:n.-121-43T>C
ENST00000525645.1:n.159-43T>C
ENST00000525803.1:c.84-43T>C ENSP00000431750.1:n.84-43T>C
ENST00000528679.5:c.84-43T>C ENSP00000435895.1:n.84-43T>C
ENST00000531673.5:c.84-43T>C ENSP00000433469.1:n.84-43T>C
NM_000317.2:c.84-43T>C NP_000308.1:n.84-43T>C
NM_000317.3:c.84-43T>C MANE Select NP_000308.1:n.84-43T>C