Canonical Allele Identifier: CA2617354192

Gene: TPI1

Linked Data

• gnomAD v4: 12-6869896-CTTGTCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869897_6869903del , CM000674.2:g.6869897_6869903del	GRCh38
NC_000012.11:g.6979061_6979067del , CM000674.1:g.6979061_6979067del	GRCh37
NC_000012.10:g.6849322_6849328del	NCBI36
NG_011948.1:g.7478_7484del
NG_013308.1:g.8455_8461del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.543+124_543+130del MANE Select	ENSP00000379933.4:n.543+124_543+130del
ENST00000229270.8:c.654+124_654+130del	ENSP00000229270.4:n.654+124_654+130del
ENST00000396705.9:c.543+124_543+130del	ENSP00000379933.4:n.543+124_543+130del
ENST00000482209.1:n.226+124_226+130del
ENST00000488464.6:c.297+124_297+130del	ENSP00000475620.1:n.297+124_297+130del
ENST00000493987.5:c.297+124_297+130del	ENSP00000475364.1:n.297+124_297+130del
ENST00000535434.5:c.297+124_297+130del	ENSP00000443599.1:n.297+124_297+130del
ENST00000613953.4:c.654+124_654+130del	ENSP00000484435.1:n.654+124_654+130del
NM_000365.5:c.543+124_543+130del	NP_000356.1:n.543+124_543+130del
NM_001159287.1:c.654+124_654+130del	NP_001152759.1:n.654+124_654+130del
NM_001258026.1:c.297+124_297+130del	NP_001244955.1:n.297+124_297+130del
XR_002957378.1:n.1400_1406del
NM_000365.6:c.543+124_543+130del MANE Select	NP_000356.1:n.543+124_543+130del
NM_001258026.2:c.297+124_297+130del	NP_001244955.1:n.297+124_297+130del