Canonical Allele Identifier: CA2014289642

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870323C= , CM000674.2:g.6870323C=	GRCh38
NC_000012.11:g.6979487C= , CM000674.1:g.6979487C=	GRCh37
NC_000012.10:g.6849748C=	NCBI36
NG_011948.1:g.7904C=
NG_013308.1:g.8035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.690C= MANE Select	ENSP00000379933.4:p.Phe230=
ENST00000229270.8:c.801C=	ENSP00000229270.4:p.Phe267=
ENST00000396705.9:c.690C=	ENSP00000379933.4:p.Phe230=
ENST00000474253.1:n.179C=
ENST00000488464.6:c.444C=	ENSP00000475620.1:p.Phe148=
ENST00000535434.5:c.444C=	ENSP00000443599.1:p.Phe148=
ENST00000613953.4:c.801C=	ENSP00000484435.1:p.Phe267=
NM_000365.5:c.690C=	NP_000356.1:p.Phe230=
NM_001159287.1:c.801C=	NP_001152759.1:p.Phe267=
NM_001258026.1:c.444C=	NP_001244955.1:p.Phe148=
XR_002957378.1:n.1698C=
NM_000365.6:c.690C= MANE Select	NP_000356.1:p.Phe230=
NM_001258026.2:c.444C=	NP_001244955.1:p.Phe148=