Canonical Allele Identifier: CA2615999735

Gene: PTS

Linked Data

• gnomAD v4: 11-112228556-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228556C>A , CM000673.2:g.112228556C>A	GRCh38
NC_000011.9:g.112099279C>A , CM000673.1:g.112099279C>A	GRCh37
NC_000011.8:g.111604489C>A	NCBI36
NG_008743.1:g.7192C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.84-38C>A MANE Select	ENSP00000280362.3:n.84-38C>A
ENST00000280362.7:c.84-38C>A	ENSP00000280362.3:n.84-38C>A
ENST00000524931.1:c.-121-38C>A	ENSP00000434688.1:n.-121-38C>A
ENST00000525645.1:n.159-38C>A
ENST00000525803.1:c.84-38C>A	ENSP00000431750.1:n.84-38C>A
ENST00000528679.5:c.84-38C>A	ENSP00000435895.1:n.84-38C>A
ENST00000531673.5:c.84-38C>A	ENSP00000433469.1:n.84-38C>A
NM_000317.2:c.84-38C>A	NP_000308.1:n.84-38C>A
NM_000317.3:c.84-38C>A MANE Select	NP_000308.1:n.84-38C>A