Canonical Allele Identifier: CA382627885
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112103939C>G (hg19) chr11:g.112233216C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233216C>G , CM000673.2:g.112233216C>G GRCh38
NC_000011.9:g.112103939C>G , CM000673.1:g.112103939C>G GRCh37
NC_000011.8:g.111609149C>G NCBI36
NG_008743.1:g.11852C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.297C>G MANE Select ENSP00000280362.3:p.Tyr99Ter
ENST00000280362.7:c.297C>G ENSP00000280362.3:p.Tyr99Ter
ENST00000524931.1:c.93C>G ENSP00000434688.1:p.Tyr31Ter
ENST00000525803.1:c.*31C>G ENSP00000431750.1:n.*31C>G
ENST00000527428.5:n.471C>G
ENST00000527635.1:n.338C>G
ENST00000528679.5:c.*106C>G ENSP00000435895.1:n.*106C>G
ENST00000531175.1:n.248C>G
ENST00000531673.5:c.*106C>G ENSP00000433469.1:n.*106C>G
NM_000317.2:c.297C>G NP_000308.1:p.Tyr99Ter
XM_011542943.1:c.258C>G XP_011541245.1:p.Tyr86Ter
NM_000317.3:c.297C>G MANE Select NP_000308.1:p.Tyr99Ter
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