Canonical Allele Identifier: CA383714390
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870375A>T , CM000674.2:g.6870375A>T GRCh38
NC_000012.11:g.6979539A>T , CM000674.1:g.6979539A>T GRCh37
NC_000012.10:g.6849800A>T NCBI36
NG_011948.1:g.7956A>T
NG_013308.1:g.7983T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.742A>T MANE Select ENSP00000379933.4:p.Lys248Ter
ENST00000229270.8:c.853A>T ENSP00000229270.4:p.Lys285Ter
ENST00000396705.9:c.742A>T ENSP00000379933.4:p.Lys248Ter
ENST00000474253.1:n.231A>T
ENST00000488464.6:c.496A>T ENSP00000475620.1:p.Lys166Ter
ENST00000535434.5:c.496A>T ENSP00000443599.1:p.Lys166Ter
ENST00000613953.4:c.853A>T ENSP00000484435.1:p.Lys285Ter
NM_000365.5:c.742A>T NP_000356.1:p.Lys248Ter
NM_001159287.1:c.853A>T NP_001152759.1:p.Lys285Ter
NM_001258026.1:c.496A>T NP_001244955.1:p.Lys166Ter
XR_002957378.1:n.1750A>T
NM_000365.6:c.742A>T MANE Select NP_000356.1:p.Lys248Ter
NM_001258026.2:c.496A>T NP_001244955.1:p.Lys166Ter