Canonical Allele Identifier: CA671775099

Gene: PTS

Linked Data

• dbSNP Id: rs374541778
• gnomAD v3: 11-112233150-G-A
• gnomAD v4: 11-112233150-G-A
• MyVariant Identifiers: chr11:g.112103873G>A (hg19) ; chr11:g.112233150G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233150G>A , CM000673.2:g.112233150G>A	GRCh38
NC_000011.9:g.112103873G>A , CM000673.1:g.112103873G>A	GRCh37
NC_000011.8:g.111609083G>A	NCBI36
NG_008743.1:g.11786G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.244-13G>A MANE Select	ENSP00000280362.3:n.244-13G>A
ENST00000280362.7:c.244-13G>A	ENSP00000280362.3:n.244-13G>A
ENST00000524931.1:c.40-13G>A	ENSP00000434688.1:n.40-13G>A
ENST00000525803.1:c.164-13G>A	ENSP00000431750.1:n.164-13G>A
ENST00000527428.5:n.418-13G>A
ENST00000527635.1:n.285-13G>A
ENST00000528679.5:c.*53-13G>A	ENSP00000435895.1:n.*53-13G>A
ENST00000531175.1:n.195-13G>A
ENST00000531673.5:c.*53-13G>A	ENSP00000433469.1:n.*53-13G>A
NM_000317.2:c.244-13G>A	NP_000308.1:n.244-13G>A
XM_011542943.1:c.205-13G>A	XP_011541245.1:n.205-13G>A
NM_000317.3:c.244-13G>A MANE Select	NP_000308.1:n.244-13G>A