Canonical Allele Identifier: CA2014289625

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870275T= , CM000674.2:g.6870275T=	GRCh38
NC_000012.11:g.6979439T= , CM000674.1:g.6979439T=	GRCh37
NC_000012.10:g.6849700T=	NCBI36
NG_011948.1:g.7856T=
NG_013308.1:g.8083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.642T= MANE Select	ENSP00000379933.4:p.Thr214=
ENST00000229270.8:c.753T=	ENSP00000229270.4:p.Thr251=
ENST00000396705.9:c.642T=	ENSP00000379933.4:p.Thr214=
ENST00000474253.1:n.131T=
ENST00000488464.6:c.396T=	ENSP00000475620.1:p.Thr132=
ENST00000535434.5:c.396T=	ENSP00000443599.1:p.Thr132=
ENST00000613953.4:c.753T=	ENSP00000484435.1:p.Thr251=
NM_000365.5:c.642T=	NP_000356.1:p.Thr214=
NM_001159287.1:c.753T=	NP_001152759.1:p.Thr251=
NM_001258026.1:c.396T=	NP_001244955.1:p.Thr132=
XR_002957378.1:n.1650T=
NM_000365.6:c.642T= MANE Select	NP_000356.1:p.Thr214=
NM_001258026.2:c.396T=	NP_001244955.1:p.Thr132=