Canonical Allele Identifier: CA2014289440
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869929T= , CM000674.2:g.6869929T= GRCh38
NC_000012.11:g.6979093T= , CM000674.1:g.6979093T= GRCh37
NC_000012.10:g.6849354T= NCBI36
NG_011948.1:g.7510T=
NG_013308.1:g.8429A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.544-120T= MANE Select ENSP00000379933.4:n.544-120T=
ENST00000229270.8:c.655-120T= ENSP00000229270.4:n.655-120T=
ENST00000396705.9:c.544-120T= ENSP00000379933.4:n.544-120T=
ENST00000482209.1:n.227-107T=
ENST00000488464.6:c.298-120T= ENSP00000475620.1:n.298-120T=
ENST00000493987.5:c.298-120T= ENSP00000475364.1:n.298-120T=
ENST00000535434.5:c.298-120T= ENSP00000443599.1:n.298-120T=
ENST00000613953.4:c.655-120T= ENSP00000484435.1:n.655-120T=
NM_000365.5:c.544-120T= NP_000356.1:n.544-120T=
NM_001159287.1:c.655-120T= NP_001152759.1:n.655-120T=
NM_001258026.1:c.298-120T= NP_001244955.1:n.298-120T=
XR_002957378.1:n.1432T=
NM_000365.6:c.544-120T= MANE Select NP_000356.1:n.544-120T=
NM_001258026.2:c.298-120T= NP_001244955.1:n.298-120T=