Canonical Allele Identifier: CA2014289640
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870312G= , CM000674.2:g.6870312G= GRCh38
NC_000012.11:g.6979476G= , CM000674.1:g.6979476G= GRCh37
NC_000012.10:g.6849737G= NCBI36
NG_011948.1:g.7893G=
NG_013308.1:g.8046C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.679G= MANE Select ENSP00000379933.4:p.Val227=
ENST00000229270.8:c.790G= ENSP00000229270.4:p.Val264=
ENST00000396705.9:c.679G= ENSP00000379933.4:p.Val227=
ENST00000474253.1:n.168G=
ENST00000488464.6:c.433G= ENSP00000475620.1:p.Val145=
ENST00000535434.5:c.433G= ENSP00000443599.1:p.Val145=
ENST00000613953.4:c.790G= ENSP00000484435.1:p.Val264=
NM_000365.5:c.679G= NP_000356.1:p.Val227=
NM_001159287.1:c.790G= NP_001152759.1:p.Val264=
NM_001258026.1:c.433G= NP_001244955.1:p.Val145=
XR_002957378.1:n.1687G=
NM_000365.6:c.679G= MANE Select NP_000356.1:p.Val227=
NM_001258026.2:c.433G= NP_001244955.1:p.Val145=