Canonical Allele Identifier: CA382627109
Gene: PTS HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.152A>T MANE Select ENSP00000280362.3:p.His51Leu
ENST00000280362.7:c.152A>T ENSP00000280362.3:p.His51Leu
ENST00000524931.1:c.-53A>T ENSP00000434688.1:n.-53A>T
ENST00000525645.1:n.227A>T
ENST00000525803.1:c.152A>T ENSP00000431750.1:p.His51Leu
ENST00000528679.5:c.152A>T ENSP00000435895.1:p.His51Leu
ENST00000531673.5:c.152A>T ENSP00000433469.1:p.His51Leu
NM_000317.2:c.152A>T NP_000308.1:p.His51Leu
NM_000317.3:c.152A>T MANE Select NP_000308.1:p.His51Leu