Canonical Allele Identifier: CA2617355040

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870222-T-TGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870222_6870223insGCCC , CM000674.2:g.6870222_6870223insGCCC	GRCh38
NC_000012.11:g.6979386_6979387insGCCC , CM000674.1:g.6979386_6979387insGCCC	GRCh37
NC_000012.10:g.6849647_6849648insGCCC	NCBI36
NG_011948.1:g.7803_7804insGCCC
NG_013308.1:g.8135_8136insGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.632-43_632-42insGCCC MANE Select	ENSP00000379933.4:n.632-43_632-42insGCCC
ENST00000229270.8:c.743-43_743-42insGCCC	ENSP00000229270.4:n.743-43_743-42insGCCC
ENST00000396705.9:c.632-43_632-42insGCCC	ENSP00000379933.4:n.632-43_632-42insGCCC
ENST00000474253.1:n.121-43_121-42insGCCC
ENST00000488464.6:c.386-43_386-42insGCCC	ENSP00000475620.1:n.386-43_386-42insGCCC
ENST00000535434.5:c.386-43_386-42insGCCC	ENSP00000443599.1:n.386-43_386-42insGCCC
ENST00000613953.4:c.743-43_743-42insGCCC	ENSP00000484435.1:n.743-43_743-42insGCCC
NM_000365.5:c.632-43_632-42insGCCC	NP_000356.1:n.632-43_632-42insGCCC
NM_001159287.1:c.743-43_743-42insGCCC	NP_001152759.1:n.743-43_743-42insGCCC
NM_001258026.1:c.386-43_386-42insGCCC	NP_001244955.1:n.386-43_386-42insGCCC
XR_002957378.1:n.1640-43_1640-42insGCCC
NM_000365.6:c.632-43_632-42insGCCC MANE Select	NP_000356.1:n.632-43_632-42insGCCC
NM_001258026.2:c.386-43_386-42insGCCC	NP_001244955.1:n.386-43_386-42insGCCC