Canonical Allele Identifier: CA2838434513
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870434dup , CM000674.2:g.6870434dup GRCh38
NC_000012.11:g.6979598dup , CM000674.1:g.6979598dup GRCh37
NC_000012.10:g.6849859dup NCBI36
NG_011948.1:g.8015dup
NG_013308.1:g.7926dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*51dup MANE Select ENSP00000379933.4:n.*51dup
ENST00000229270.8:c.*51dup ENSP00000229270.4:n.*51dup
ENST00000396705.9:c.*51dup ENSP00000379933.4:n.*51dup
ENST00000474253.1:n.290dup
ENST00000535434.5:c.*51dup ENSP00000443599.1:n.*51dup
ENST00000613953.4:c.*51dup ENSP00000484435.1:n.*51dup
NM_000365.5:c.*51dup NP_000356.1:n.*51dup
NM_001159287.1:c.*51dup NP_001152759.1:n.*51dup
NM_001258026.1:c.*51dup NP_001244955.1:n.*51dup
XR_002957378.1:n.1809dup
NM_000365.6:c.*51dup MANE Select NP_000356.1:n.*51dup
NM_001258026.2:c.*51dup NP_001244955.1:n.*51dup