Canonical Allele Identifier: CA2014289644
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870328T= , CM000674.2:g.6870328T= GRCh38
NC_000012.11:g.6979492T= , CM000674.1:g.6979492T= GRCh37
NC_000012.10:g.6849753T= NCBI36
NG_011948.1:g.7909T=
NG_013308.1:g.8030A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.695T= MANE Select ENSP00000379933.4:p.Val232=
ENST00000229270.8:c.806T= ENSP00000229270.4:p.Val269=
ENST00000396705.9:c.695T= ENSP00000379933.4:p.Val232=
ENST00000474253.1:n.184T=
ENST00000488464.6:c.449T= ENSP00000475620.1:p.Val150=
ENST00000535434.5:c.449T= ENSP00000443599.1:p.Val150=
ENST00000613953.4:c.806T= ENSP00000484435.1:p.Val269=
NM_000365.5:c.695T= NP_000356.1:p.Val232=
NM_001159287.1:c.806T= NP_001152759.1:p.Val269=
NM_001258026.1:c.449T= NP_001244955.1:p.Val150=
XR_002957378.1:n.1703T=
NM_000365.6:c.695T= MANE Select NP_000356.1:p.Val232=
NM_001258026.2:c.449T= NP_001244955.1:p.Val150=