Canonical Allele Identifier: CA2014289402

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869847G= , CM000674.2:g.6869847G=	GRCh38
NC_000012.11:g.6979011G= , CM000674.1:g.6979011G=	GRCh37
NC_000012.10:g.6849272G=	NCBI36
NG_011948.1:g.7428G=
NG_013308.1:g.8511C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.543+74G= MANE Select	ENSP00000379933.4:n.543+74G=
ENST00000229270.8:c.654+74G=	ENSP00000229270.4:n.654+74G=
ENST00000396705.9:c.543+74G=	ENSP00000379933.4:n.543+74G=
ENST00000482209.1:n.226+74G=
ENST00000488464.6:c.297+74G=	ENSP00000475620.1:n.297+74G=
ENST00000493987.5:c.297+74G=	ENSP00000475364.1:n.297+74G=
ENST00000535434.5:c.297+74G=	ENSP00000443599.1:n.297+74G=
ENST00000613953.4:c.654+74G=	ENSP00000484435.1:n.654+74G=
NM_000365.5:c.543+74G=	NP_000356.1:n.543+74G=
NM_001159287.1:c.654+74G=	NP_001152759.1:n.654+74G=
NM_001258026.1:c.297+74G=	NP_001244955.1:n.297+74G=
XR_002957378.1:n.1350G=
NM_000365.6:c.543+74G= MANE Select	NP_000356.1:n.543+74G=
NM_001258026.2:c.297+74G=	NP_001244955.1:n.297+74G=