Canonical Allele Identifier: CA2615999653
Gene: PTS HGNC NCBI

Linked Data

gnomAD v4: 11-112228485-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112228485A>G , CM000673.2:g.112228485A>G GRCh38
NC_000011.9:g.112099208A>G , CM000673.1:g.112099208A>G GRCh37
NC_000011.8:g.111604418A>G NCBI36
NG_008743.1:g.7121A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000280362.8:c.84-109A>G MANE Select ENSP00000280362.3:n.84-109A>G
ENST00000280362.7:c.84-109A>G ENSP00000280362.3:n.84-109A>G
ENST00000524931.1:c.-121-109A>G ENSP00000434688.1:n.-121-109A>G
ENST00000525645.1:n.159-109A>G
ENST00000525803.1:c.84-109A>G ENSP00000431750.1:n.84-109A>G
ENST00000528679.5:c.84-109A>G ENSP00000435895.1:n.84-109A>G
ENST00000531673.5:c.84-109A>G ENSP00000433469.1:n.84-109A>G
NM_000317.2:c.84-109A>G NP_000308.1:n.84-109A>G
NM_000317.3:c.84-109A>G MANE Select NP_000308.1:n.84-109A>G
Search 100 bp 5'
Search 100 bp 3'