Canonical Allele Identifier: CA2014289647

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870337_6870338delinsCT , CM000674.2:g.6870337_6870338delinsCT	GRCh38
NC_000012.11:g.6979501_6979502delinsCT , CM000674.1:g.6979501_6979502delinsCT	GRCh37
NC_000012.10:g.6849762_6849763delinsCT	NCBI36
NG_011948.1:g.7918_7919delinsCT
NG_013308.1:g.8020_8021delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.704_705delinsCT MANE Select	ENSP00000379933.4:p.Ala235=
ENST00000229270.8:c.815_816delinsCT	ENSP00000229270.4:p.Ala272=
ENST00000396705.9:c.704_705delinsCT	ENSP00000379933.4:p.Ala235=
ENST00000474253.1:n.193_194delinsCT
ENST00000488464.6:c.458_459delinsCT	ENSP00000475620.1:p.Ala153=
ENST00000535434.5:c.458_459delinsCT	ENSP00000443599.1:p.Ala153=
ENST00000613953.4:c.815_816delinsCT	ENSP00000484435.1:p.Ala272=
NM_000365.5:c.704_705delinsCT	NP_000356.1:p.Ala235=
NM_001159287.1:c.815_816delinsCT	NP_001152759.1:p.Ala272=
NM_001258026.1:c.458_459delinsCT	NP_001244955.1:p.Ala153=
XR_002957378.1:n.1712_1713delinsCT
NM_000365.6:c.704_705delinsCT MANE Select	NP_000356.1:p.Ala235=
NM_001258026.2:c.458_459delinsCT	NP_001244955.1:p.Ala153=