Canonical Allele Identifier: CA2014289770

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870552T= , CM000674.2:g.6870552T=	GRCh38
NC_000012.11:g.6979716T= , CM000674.1:g.6979716T=	GRCh37
NC_000012.10:g.6849977T=	NCBI36
NG_011948.1:g.8133T=
NG_013308.1:g.7806A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*169T= MANE Select	ENSP00000379933.4:n.*169T=
ENST00000229270.8:c.*169T=	ENSP00000229270.4:n.*169T=
ENST00000396705.9:c.*169T=	ENSP00000379933.4:n.*169T=
ENST00000474253.1:n.408T=
ENST00000535434.5:c.*169T=	ENSP00000443599.1:n.*169T=
ENST00000613953.4:c.*169T=	ENSP00000484435.1:n.*169T=
NM_000365.5:c.*169T=	NP_000356.1:n.*169T=
NM_001159287.1:c.*169T=	NP_001152759.1:n.*169T=
NM_001258026.1:c.*169T=	NP_001244955.1:n.*169T=
XR_002957378.1:n.1927T=
NM_000365.6:c.*169T= MANE Select	NP_000356.1:n.*169T=
NM_001258026.2:c.*169T=	NP_001244955.1:n.*169T=