Canonical Allele Identifier: CA2014289686
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870408C= , CM000674.2:g.6870408C= GRCh38
NC_000012.11:g.6979572C= , CM000674.1:g.6979572C= GRCh37
NC_000012.10:g.6849833C= NCBI36
NG_011948.1:g.7989C=
NG_013308.1:g.7950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*25C= MANE Select ENSP00000379933.4:n.*25C=
ENST00000229270.8:c.*25C= ENSP00000229270.4:n.*25C=
ENST00000396705.9:c.*25C= ENSP00000379933.4:n.*25C=
ENST00000474253.1:n.264C=
ENST00000535434.5:c.*25C= ENSP00000443599.1:n.*25C=
ENST00000613953.4:c.*25C= ENSP00000484435.1:n.*25C=
NM_000365.5:c.*25C= NP_000356.1:n.*25C=
NM_001159287.1:c.*25C= NP_001152759.1:n.*25C=
NM_001258026.1:c.*25C= NP_001244955.1:n.*25C=
XR_002957378.1:n.1783C=
NM_000365.6:c.*25C= MANE Select NP_000356.1:n.*25C=
NM_001258026.2:c.*25C= NP_001244955.1:n.*25C=