Canonical Allele Identifier: CA382627073
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112099367A>C (hg19) chr11:g.112228644A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228644A>C , CM000673.2:g.112228644A>C GRCh38
NC_000011.9:g.112099367A>C , CM000673.1:g.112099367A>C GRCh37
NC_000011.8:g.111604577A>C NCBI36
NG_008743.1:g.7280A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.134A>C MANE Select ENSP00000280362.3:p.Asn45Thr
ENST00000280362.7:c.134A>C ENSP00000280362.3:p.Asn45Thr
ENST00000524931.1:c.-71A>C ENSP00000434688.1:n.-71A>C
ENST00000525645.1:n.209A>C
ENST00000525803.1:c.134A>C ENSP00000431750.1:p.Asn45Thr
ENST00000528679.5:c.134A>C ENSP00000435895.1:p.Asn45Thr
ENST00000531673.5:c.134A>C ENSP00000433469.1:p.Asn45Thr
NM_000317.2:c.134A>C NP_000308.1:p.Asn45Thr
NM_000317.3:c.134A>C MANE Select NP_000308.1:p.Asn45Thr
Search 100 bp 5'
Search 100 bp 3'