Canonical Allele Identifier: CA2617354258

Gene: TPI1

Linked Data

• dbSNP Id: rs2138094218
• gnomAD v4: 12-6869919-GGGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869923_6869927del , CM000674.2:g.6869923_6869927del	GRCh38
NC_000012.11:g.6979087_6979091del , CM000674.1:g.6979087_6979091del	GRCh37
NC_000012.10:g.6849348_6849352del	NCBI36
NG_011948.1:g.7504_7508del
NG_013308.1:g.8434_8438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.544-126_544-122del MANE Select	ENSP00000379933.4:n.544-126_544-122del
ENST00000229270.8:c.655-126_655-122del	ENSP00000229270.4:n.655-126_655-122del
ENST00000396705.9:c.544-126_544-122del	ENSP00000379933.4:n.544-126_544-122del
ENST00000482209.1:n.227-113_227-109del
ENST00000488464.6:c.298-126_298-122del	ENSP00000475620.1:n.298-126_298-122del
ENST00000493987.5:c.298-126_298-122del	ENSP00000475364.1:n.298-126_298-122del
ENST00000535434.5:c.298-126_298-122del	ENSP00000443599.1:n.298-126_298-122del
ENST00000613953.4:c.655-126_655-122del	ENSP00000484435.1:n.655-126_655-122del
NM_000365.5:c.544-126_544-122del	NP_000356.1:n.544-126_544-122del
NM_001159287.1:c.655-126_655-122del	NP_001152759.1:n.655-126_655-122del
NM_001258026.1:c.298-126_298-122del	NP_001244955.1:n.298-126_298-122del
XR_002957378.1:n.1426_1430del
NM_000365.6:c.544-126_544-122del MANE Select	NP_000356.1:n.544-126_544-122del
NM_001258026.2:c.298-126_298-122del	NP_001244955.1:n.298-126_298-122del