Canonical Allele Identifier: CA944389648

Gene: TPI1

Linked Data

• dbSNP Id: rs1944550565
• gnomAD v3: 12-6869970-C-CT
• gnomAD v4: 12-6869970-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869971dup , CM000674.2:g.6869971dup	GRCh38
NC_000012.11:g.6979135dup , CM000674.1:g.6979135dup	GRCh37
NC_000012.10:g.6849396dup	NCBI36
NG_011948.1:g.7552dup
NG_013308.1:g.8387dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.544-78dup MANE Select	ENSP00000379933.4:n.544-78dup
ENST00000229270.8:c.655-78dup	ENSP00000229270.4:n.655-78dup
ENST00000396705.9:c.544-78dup	ENSP00000379933.4:n.544-78dup
ENST00000482209.1:n.227-65dup
ENST00000488464.6:c.298-78dup	ENSP00000475620.1:n.298-78dup
ENST00000493987.5:c.298-78dup	ENSP00000475364.1:n.298-78dup
ENST00000535434.5:c.298-78dup	ENSP00000443599.1:n.298-78dup
ENST00000613953.4:c.655-78dup	ENSP00000484435.1:n.655-78dup
NM_000365.5:c.544-78dup	NP_000356.1:n.544-78dup
NM_001159287.1:c.655-78dup	NP_001152759.1:n.655-78dup
NM_001258026.1:c.298-78dup	NP_001244955.1:n.298-78dup
XR_002957378.1:n.1474dup
NM_000365.6:c.544-78dup MANE Select	NP_000356.1:n.544-78dup
NM_001258026.2:c.298-78dup	NP_001244955.1:n.298-78dup