Canonical Allele Identifier: CA2014289515
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870064G= , CM000674.2:g.6870064G= GRCh38
NC_000012.11:g.6979228G= , CM000674.1:g.6979228G= GRCh37
NC_000012.10:g.6849489G= NCBI36
NG_011948.1:g.7645G=
NG_013308.1:g.8294C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.559G= MANE Select ENSP00000379933.4:p.Glu187=
ENST00000229270.8:c.670G= ENSP00000229270.4:p.Glu224=
ENST00000396705.9:c.559G= ENSP00000379933.4:p.Glu187=
ENST00000474253.1:n.48G=
ENST00000482209.1:n.255G=
ENST00000488464.6:c.313G= ENSP00000475620.1:p.Glu105=
ENST00000493987.5:c.313G= ENSP00000475364.1:p.Glu105=
ENST00000535434.5:c.313G= ENSP00000443599.1:p.Glu105=
ENST00000613953.4:c.670G= ENSP00000484435.1:p.Glu224=
NM_000365.5:c.559G= NP_000356.1:p.Glu187=
NM_001159287.1:c.670G= NP_001152759.1:p.Glu224=
NM_001258026.1:c.313G= NP_001244955.1:p.Glu105=
XR_002957378.1:n.1567G=
NM_000365.6:c.559G= MANE Select NP_000356.1:p.Glu187=
NM_001258026.2:c.313G= NP_001244955.1:p.Glu105=