Canonical Allele Identifier: CA382627094
Gene: PTS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228653G>C , CM000673.2:g.112228653G>C GRCh38
NC_000011.9:g.112099376G>C , CM000673.1:g.112099376G>C GRCh37
NC_000011.8:g.111604586G>C NCBI36
NG_008743.1:g.7289G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.143G>C MANE Select ENSP00000280362.3:p.Gly48Ala
ENST00000280362.7:c.143G>C ENSP00000280362.3:p.Gly48Ala
ENST00000524931.1:c.-62G>C ENSP00000434688.1:n.-62G>C
ENST00000525645.1:n.218G>C
ENST00000525803.1:c.143G>C ENSP00000431750.1:p.Gly48Ala
ENST00000528679.5:c.143G>C ENSP00000435895.1:p.Gly48Ala
ENST00000531673.5:c.143G>C ENSP00000433469.1:p.Gly48Ala
NM_000317.2:c.143G>C NP_000308.1:p.Gly48Ala
NM_000317.3:c.143G>C MANE Select NP_000308.1:p.Gly48Ala