Canonical Allele Identifier: CA2014289664

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870363A= , CM000674.2:g.6870363A=	GRCh38
NC_000012.11:g.6979527A= , CM000674.1:g.6979527A=	GRCh37
NC_000012.10:g.6849788A=	NCBI36
NG_011948.1:g.7944A=
NG_013308.1:g.7995T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.730A= MANE Select	ENSP00000379933.4:p.Ile244=
ENST00000229270.8:c.841A=	ENSP00000229270.4:p.Ile281=
ENST00000396705.9:c.730A=	ENSP00000379933.4:p.Ile244=
ENST00000474253.1:n.219A=
ENST00000488464.6:c.484A=	ENSP00000475620.1:p.Ile162=
ENST00000535434.5:c.484A=	ENSP00000443599.1:p.Ile162=
ENST00000613953.4:c.841A=	ENSP00000484435.1:p.Ile281=
NM_000365.5:c.730A=	NP_000356.1:p.Ile244=
NM_001159287.1:c.841A=	NP_001152759.1:p.Ile281=
NM_001258026.1:c.484A=	NP_001244955.1:p.Ile162=
XR_002957378.1:n.1738A=
NM_000365.6:c.730A= MANE Select	NP_000356.1:p.Ile244=
NM_001258026.2:c.484A=	NP_001244955.1:p.Ile162=