Canonical Allele Identifier: CA2617355971

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870668-C-CTTTGAAAAAATGTTTTGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870669_6870670insTTGAAAAAATGTTTTGCGT , CM000674.2:g.6870669_6870670insTTGAAAAAATGTTTTGCGT	GRCh38
NC_000012.11:g.6979833_6979834insTTGAAAAAATGTTTTGCGT , CM000674.1:g.6979833_6979834insTTGAAAAAATGTTTTGCGT	GRCh37
NC_000012.10:g.6850094_6850095insTTGAAAAAATGTTTTGCGT	NCBI36
NG_011948.1:g.8250_8251insTTGAAAAAATGTTTTGCGT
NG_013308.1:g.7689_7690insCGCAAAACATTTTTTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*286_*287insTTGAAAAAATGTTTTGCGT MANE Select	ENSP00000379933.4:n.*286_*287insTTGAAAAAATGTTTTGCGT
ENST00000229270.8:c.*286_*287insTTGAAAAAATGTTTTGCGT	ENSP00000229270.4:n.*286_*287insTTGAAAAAATGTTTTGCGT
ENST00000396705.9:c.*286_*287insTTGAAAAAATGTTTTGCGT	ENSP00000379933.4:n.*286_*287insTTGAAAAAATGTTTTGCGT
ENST00000535434.5:c.*286_*287insTTGAAAAAATGTTTTGCGT	ENSP00000443599.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
ENST00000613953.4:c.*286_*287insTTGAAAAAATGTTTTGCGT	ENSP00000484435.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
NM_000365.5:c.*286_*287insTTGAAAAAATGTTTTGCGT	NP_000356.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
NM_001159287.1:c.*286_*287insTTGAAAAAATGTTTTGCGT	NP_001152759.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
NM_001258026.1:c.*286_*287insTTGAAAAAATGTTTTGCGT	NP_001244955.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
XR_002957378.1:n.2044_2045insTTGAAAAAATGTTTTGCGT
NM_000365.6:c.*286_*287insTTGAAAAAATGTTTTGCGT MANE Select	NP_000356.1:n.*286_*287insTTGAAAAAATGTTTTGCGT
NM_001258026.2:c.*286_*287insTTGAAAAAATGTTTTGCGT	NP_001244955.1:n.*286_*287insTTGAAAAAATGTTTTGCGT