Canonical Allele Identifier: CA2014289559

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870153C= , CM000674.2:g.6870153C=	GRCh38
NC_000012.11:g.6979317C= , CM000674.1:g.6979317C=	GRCh37
NC_000012.10:g.6849578C=	NCBI36
NG_011948.1:g.7734C=
NG_013308.1:g.8205G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.631+17C= MANE Select	ENSP00000379933.4:n.631+17C=
ENST00000229270.8:c.742+17C=	ENSP00000229270.4:n.742+17C=
ENST00000396705.9:c.631+17C=	ENSP00000379933.4:n.631+17C=
ENST00000474253.1:n.120+17C=
ENST00000488464.6:c.385+17C=	ENSP00000475620.1:n.385+17C=
ENST00000535434.5:c.385+17C=	ENSP00000443599.1:n.385+17C=
ENST00000613953.4:c.742+17C=	ENSP00000484435.1:n.742+17C=
NM_000365.5:c.631+17C=	NP_000356.1:n.631+17C=
NM_001159287.1:c.742+17C=	NP_001152759.1:n.742+17C=
NM_001258026.1:c.385+17C=	NP_001244955.1:n.385+17C=
XR_002957378.1:n.1639+17C=
NM_000365.6:c.631+17C= MANE Select	NP_000356.1:n.631+17C=
NM_001258026.2:c.385+17C=	NP_001244955.1:n.385+17C=