Canonical Allele Identifier: CA2014289420

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869882C= , CM000674.2:g.6869882C=	GRCh38
NC_000012.11:g.6979046C= , CM000674.1:g.6979046C=	GRCh37
NC_000012.10:g.6849307C=	NCBI36
NG_011948.1:g.7463C=
NG_013308.1:g.8476G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.543+109C= MANE Select	ENSP00000379933.4:n.543+109C=
ENST00000229270.8:c.654+109C=	ENSP00000229270.4:n.654+109C=
ENST00000396705.9:c.543+109C=	ENSP00000379933.4:n.543+109C=
ENST00000482209.1:n.226+109C=
ENST00000488464.6:c.297+109C=	ENSP00000475620.1:n.297+109C=
ENST00000493987.5:c.297+109C=	ENSP00000475364.1:n.297+109C=
ENST00000535434.5:c.297+109C=	ENSP00000443599.1:n.297+109C=
ENST00000613953.4:c.654+109C=	ENSP00000484435.1:n.654+109C=
NM_000365.5:c.543+109C=	NP_000356.1:n.543+109C=
NM_001159287.1:c.654+109C=	NP_001152759.1:n.654+109C=
NM_001258026.1:c.297+109C=	NP_001244955.1:n.297+109C=
XR_002957378.1:n.1385C=
NM_000365.6:c.543+109C= MANE Select	NP_000356.1:n.543+109C=
NM_001258026.2:c.297+109C=	NP_001244955.1:n.297+109C=