Canonical Allele Identifier: CA2014289646

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870335T= , CM000674.2:g.6870335T=	GRCh38
NC_000012.11:g.6979499T= , CM000674.1:g.6979499T=	GRCh37
NC_000012.10:g.6849760T=	NCBI36
NG_011948.1:g.7916T=
NG_013308.1:g.8023A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.702T= MANE Select	ENSP00000379933.4:p.Gly234=
ENST00000229270.8:c.813T=	ENSP00000229270.4:p.Gly271=
ENST00000396705.9:c.702T=	ENSP00000379933.4:p.Gly234=
ENST00000474253.1:n.191T=
ENST00000488464.6:c.456T=	ENSP00000475620.1:p.Gly152=
ENST00000535434.5:c.456T=	ENSP00000443599.1:p.Gly152=
ENST00000613953.4:c.813T=	ENSP00000484435.1:p.Gly271=
NM_000365.5:c.702T=	NP_000356.1:p.Gly234=
NM_001159287.1:c.813T=	NP_001152759.1:p.Gly271=
NM_001258026.1:c.456T=	NP_001244955.1:p.Gly152=
XR_002957378.1:n.1710T=
NM_000365.6:c.702T= MANE Select	NP_000356.1:p.Gly234=
NM_001258026.2:c.456T=	NP_001244955.1:p.Gly152=