Canonical Allele Identifier: CA2504949139
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870391C>A , CM000674.2:g.6870391C>A GRCh38
NC_000012.11:g.6979555C>A , CM000674.1:g.6979555C>A GRCh37
NC_000012.10:g.6849816C>A NCBI36
NG_011948.1:g.7972C>A
NG_013308.1:g.7967G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*8C>A MANE Select ENSP00000379933.4:n.*8C>A
ENST00000229270.8:c.*8C>A ENSP00000229270.4:n.*8C>A
ENST00000396705.9:c.*8C>A ENSP00000379933.4:n.*8C>A
ENST00000474253.1:n.247C>A
ENST00000535434.5:c.*8C>A ENSP00000443599.1:n.*8C>A
ENST00000613953.4:c.*8C>A ENSP00000484435.1:n.*8C>A
NM_000365.5:c.*8C>A NP_000356.1:n.*8C>A
NM_001159287.1:c.*8C>A NP_001152759.1:n.*8C>A
NM_001258026.1:c.*8C>A NP_001244955.1:n.*8C>A
XR_002957378.1:n.1766C>A
NM_000365.6:c.*8C>A MANE Select NP_000356.1:n.*8C>A
NM_001258026.2:c.*8C>A NP_001244955.1:n.*8C>A