Canonical Allele Identifier: CA2014289424

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869890C= , CM000674.2:g.6869890C=	GRCh38
NC_000012.11:g.6979054C= , CM000674.1:g.6979054C=	GRCh37
NC_000012.10:g.6849315C=	NCBI36
NG_011948.1:g.7471C=
NG_013308.1:g.8468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.543+117C= MANE Select	ENSP00000379933.4:n.543+117C=
ENST00000229270.8:c.654+117C=	ENSP00000229270.4:n.654+117C=
ENST00000396705.9:c.543+117C=	ENSP00000379933.4:n.543+117C=
ENST00000482209.1:n.226+117C=
ENST00000488464.6:c.297+117C=	ENSP00000475620.1:n.297+117C=
ENST00000493987.5:c.297+117C=	ENSP00000475364.1:n.297+117C=
ENST00000535434.5:c.297+117C=	ENSP00000443599.1:n.297+117C=
ENST00000613953.4:c.654+117C=	ENSP00000484435.1:n.654+117C=
NM_000365.5:c.543+117C=	NP_000356.1:n.543+117C=
NM_001159287.1:c.654+117C=	NP_001152759.1:n.654+117C=
NM_001258026.1:c.297+117C=	NP_001244955.1:n.297+117C=
XR_002957378.1:n.1393C=
NM_000365.6:c.543+117C= MANE Select	NP_000356.1:n.543+117C=
NM_001258026.2:c.297+117C=	NP_001244955.1:n.297+117C=