Canonical Allele Identifier: CA382626500
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112097225T>C (hg19) chr11:g.112226502T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112226502T>C , CM000673.2:g.112226502T>C GRCh38
NC_000011.9:g.112097225T>C , CM000673.1:g.112097225T>C GRCh37
NC_000011.8:g.111602435T>C NCBI36
NG_008743.1:g.5138T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.59T>C MANE Select ENSP00000280362.3:p.Phe20Ser
ENST00000280362.7:c.59T>C ENSP00000280362.3:p.Phe20Ser
ENST00000525645.1:n.134T>C
ENST00000525803.1:c.59T>C ENSP00000431750.1:p.Phe20Ser
ENST00000528679.5:c.59T>C ENSP00000435895.1:p.Phe20Ser
ENST00000531673.5:c.59T>C ENSP00000433469.1:p.Phe20Ser
NM_000317.2:c.59T>C NP_000308.1:p.Phe20Ser
NM_000317.3:c.59T>C MANE Select NP_000308.1:p.Phe20Ser
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