Canonical Allele Identifier: CA2615999711
Gene: PTS HGNC NCBI

Linked Data

gnomAD v4: 11-112228546-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228546G>T , CM000673.2:g.112228546G>T GRCh38
NC_000011.9:g.112099269G>T , CM000673.1:g.112099269G>T GRCh37
NC_000011.8:g.111604479G>T NCBI36
NG_008743.1:g.7182G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.84-48G>T MANE Select ENSP00000280362.3:n.84-48G>T
ENST00000280362.7:c.84-48G>T ENSP00000280362.3:n.84-48G>T
ENST00000524931.1:c.-121-48G>T ENSP00000434688.1:n.-121-48G>T
ENST00000525645.1:n.159-48G>T
ENST00000525803.1:c.84-48G>T ENSP00000431750.1:n.84-48G>T
ENST00000528679.5:c.84-48G>T ENSP00000435895.1:n.84-48G>T
ENST00000531673.5:c.84-48G>T ENSP00000433469.1:n.84-48G>T
NM_000317.2:c.84-48G>T NP_000308.1:n.84-48G>T
NM_000317.3:c.84-48G>T MANE Select NP_000308.1:n.84-48G>T
Search 100 bp 5'
Search 100 bp 3'