Canonical Allele Identifier: CA6278458
Gene: PTS HGNC NCBI

Linked Data

dbSNP Id: rs780284101
ExAC: 11:112099312 G / GTTT
MyVariant Identifiers: chr11:g.112099312_112099313insTTT (hg19) chr11:g.112228589_112228590insTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228590_112228591insTTT , CM000673.2:g.112228590_112228591insTTT GRCh38
NC_000011.9:g.112099313_112099314insTTT , CM000673.1:g.112099313_112099314insTTT GRCh37
NC_000011.8:g.111604523_111604524insTTT NCBI36
NG_008743.1:g.7226_7227insTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-4_84-3insTTT MANE Select ENSP00000280362.3:n.84-4_84-3insTTT
ENST00000280362.7:c.84-4_84-3insTTT ENSP00000280362.3:n.84-4_84-3insTTT
ENST00000524931.1:c.-121-4_-121-3insTTT ENSP00000434688.1:n.-121-4_-121-3insTTT
ENST00000525645.1:n.159-4_159-3insTTT
ENST00000525803.1:c.84-4_84-3insTTT ENSP00000431750.1:n.84-4_84-3insTTT
ENST00000528679.5:c.84-4_84-3insTTT ENSP00000435895.1:n.84-4_84-3insTTT
ENST00000531673.5:c.84-4_84-3insTTT ENSP00000433469.1:n.84-4_84-3insTTT
NM_000317.2:c.84-4_84-3insTTT NP_000308.1:n.84-4_84-3insTTT
NM_000317.3:c.84-4_84-3insTTT MANE Select NP_000308.1:n.84-4_84-3insTTT
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