Canonical Allele Identifier: CA476797315
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112099371A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228648A>C , CM000673.2:g.112228648A>C GRCh38
NC_000011.9:g.112099371A>C , CM000673.1:g.112099371A>C GRCh37
NC_000011.8:g.111604581A>C NCBI36
NG_008743.1:g.7284A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.138A>C MANE Select ENSP00000280362.3:p.Pro46=
ENST00000280362.7:c.138A>C ENSP00000280362.3:p.Pro46=
ENST00000524931.1:c.-67A>C ENSP00000434688.1:n.-67A>C
ENST00000525645.1:n.213A>C
ENST00000525803.1:c.138A>C ENSP00000431750.1:p.Pro46=
ENST00000528679.5:c.138A>C ENSP00000435895.1:p.Pro46=
ENST00000531673.5:c.138A>C ENSP00000433469.1:p.Pro46=
NM_000317.2:c.138A>C NP_000308.1:p.Pro46=
NM_000317.3:c.138A>C MANE Select NP_000308.1:p.Pro46=
Search 100 bp 5'
Search 100 bp 3'