Canonical Allele Identifier: CA2794431070

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870219_6870220insT , CM000674.2:g.6870219_6870220insT	GRCh38
NC_000012.11:g.6979383_6979384insT , CM000674.1:g.6979383_6979384insT	GRCh37
NC_000012.10:g.6849644_6849645insT	NCBI36
NG_011948.1:g.7800_7801insT
NG_013308.1:g.8138_8139insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.632-46_632-45insT MANE Select	ENSP00000379933.4:n.632-46_632-45insT
ENST00000229270.8:c.743-46_743-45insT	ENSP00000229270.4:n.743-46_743-45insT
ENST00000396705.9:c.632-46_632-45insT	ENSP00000379933.4:n.632-46_632-45insT
ENST00000474253.1:n.121-46_121-45insT
ENST00000488464.6:c.386-46_386-45insT	ENSP00000475620.1:n.386-46_386-45insT
ENST00000535434.5:c.386-46_386-45insT	ENSP00000443599.1:n.386-46_386-45insT
ENST00000613953.4:c.743-46_743-45insT	ENSP00000484435.1:n.743-46_743-45insT
NM_000365.5:c.632-46_632-45insT	NP_000356.1:n.632-46_632-45insT
NM_001159287.1:c.743-46_743-45insT	NP_001152759.1:n.743-46_743-45insT
NM_001258026.1:c.386-46_386-45insT	NP_001244955.1:n.386-46_386-45insT
XR_002957378.1:n.1640-46_1640-45insT
NM_000365.6:c.632-46_632-45insT MANE Select	NP_000356.1:n.632-46_632-45insT
NM_001258026.2:c.386-46_386-45insT	NP_001244955.1:n.386-46_386-45insT