Canonical Allele Identifier: CA476797665
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112104200A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233477A>G , CM000673.2:g.112233477A>G GRCh38
NC_000011.9:g.112104200A>G , CM000673.1:g.112104200A>G GRCh37
NC_000011.8:g.111609410A>G NCBI36
NG_008743.1:g.12113A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.360A>G MANE Select ENSP00000280362.3:p.Lys120=
ENST00000280362.7:c.360A>G ENSP00000280362.3:p.Lys120=
ENST00000524931.1:c.156A>G ENSP00000434688.1:p.Lys52=
ENST00000525803.1:c.*94A>G ENSP00000431750.1:n.*94A>G
ENST00000527428.5:n.488+244A>G
ENST00000527635.1:n.401A>G
ENST00000528679.5:c.*169A>G ENSP00000435895.1:n.*169A>G
ENST00000531673.5:c.*123+244A>G ENSP00000433469.1:n.*123+244A>G
NM_000317.2:c.360A>G NP_000308.1:p.Lys120=
XM_011542943.1:c.321A>G XP_011541245.1:p.Lys107=
NM_000317.3:c.360A>G MANE Select NP_000308.1:p.Lys120=