Canonical Allele Identifier: CA476797632
Gene: PTS HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.112104191C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233468C>T , CM000673.2:g.112233468C>T GRCh38
NC_000011.9:g.112104191C>T , CM000673.1:g.112104191C>T GRCh37
NC_000011.8:g.111609401C>T NCBI36
NG_008743.1:g.12104C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.351C>T MANE Select ENSP00000280362.3:p.Asn117=
ENST00000280362.7:c.351C>T ENSP00000280362.3:p.Asn117=
ENST00000524931.1:c.147C>T ENSP00000434688.1:p.Asn49=
ENST00000525803.1:c.*85C>T ENSP00000431750.1:n.*85C>T
ENST00000527428.5:n.488+235C>T
ENST00000527635.1:n.392C>T
ENST00000528679.5:c.*160C>T ENSP00000435895.1:n.*160C>T
ENST00000531673.5:c.*123+235C>T ENSP00000433469.1:n.*123+235C>T
NM_000317.2:c.351C>T NP_000308.1:p.Asn117=
XM_011542943.1:c.312C>T XP_011541245.1:p.Asn104=
NM_000317.3:c.351C>T MANE Select NP_000308.1:p.Asn117=