Canonical Allele Identifier: CA382627111
Gene: PTS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228662A>G , CM000673.2:g.112228662A>G GRCh38
NC_000011.9:g.112099385A>G , CM000673.1:g.112099385A>G GRCh37
NC_000011.8:g.111604595A>G NCBI36
NG_008743.1:g.7298A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.152A>G MANE Select ENSP00000280362.3:p.His51Arg
ENST00000280362.7:c.152A>G ENSP00000280362.3:p.His51Arg
ENST00000524931.1:c.-53A>G ENSP00000434688.1:n.-53A>G
ENST00000525645.1:n.227A>G
ENST00000525803.1:c.152A>G ENSP00000431750.1:p.His51Arg
ENST00000528679.5:c.152A>G ENSP00000435895.1:p.His51Arg
ENST00000531673.5:c.152A>G ENSP00000433469.1:p.His51Arg
NM_000317.2:c.152A>G NP_000308.1:p.His51Arg
NM_000317.3:c.152A>G MANE Select NP_000308.1:p.His51Arg