Canonical Allele Identifier: CA2014289849
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870684G= , CM000674.2:g.6870684G= GRCh38
NC_000012.11:g.6979848G= , CM000674.1:g.6979848G= GRCh37
NC_000012.10:g.6850109G= NCBI36
NG_011948.1:g.8265G=
NG_013308.1:g.7674C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*301G= MANE Select ENSP00000379933.4:n.*301G=
ENST00000229270.8:c.*301G= ENSP00000229270.4:n.*301G=
ENST00000396705.9:c.*301G= ENSP00000379933.4:n.*301G=
ENST00000535434.5:c.*301G= ENSP00000443599.1:n.*301G=
ENST00000613953.4:c.*301G= ENSP00000484435.1:n.*301G=
NM_000365.5:c.*301G= NP_000356.1:n.*301G=
NM_001159287.1:c.*301G= NP_001152759.1:n.*301G=
NM_001258026.1:c.*301G= NP_001244955.1:n.*301G=
XR_002957378.1:n.2059G=
NM_000365.6:c.*301G= MANE Select NP_000356.1:n.*301G=
NM_001258026.2:c.*301G= NP_001244955.1:n.*301G=