Canonical Allele Identifier: CA2014289637
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870302C= , CM000674.2:g.6870302C= GRCh38
NC_000012.11:g.6979466C= , CM000674.1:g.6979466C= GRCh37
NC_000012.10:g.6849727C= NCBI36
NG_011948.1:g.7883C=
NG_013308.1:g.8056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.669C= MANE Select ENSP00000379933.4:p.Ser223=
ENST00000229270.8:c.780C= ENSP00000229270.4:p.Ser260=
ENST00000396705.9:c.669C= ENSP00000379933.4:p.Ser223=
ENST00000474253.1:n.158C=
ENST00000488464.6:c.423C= ENSP00000475620.1:p.Ser141=
ENST00000535434.5:c.423C= ENSP00000443599.1:p.Ser141=
ENST00000613953.4:c.780C= ENSP00000484435.1:p.Ser260=
NM_000365.5:c.669C= NP_000356.1:p.Ser223=
NM_001159287.1:c.780C= NP_001152759.1:p.Ser260=
NM_001258026.1:c.423C= NP_001244955.1:p.Ser141=
XR_002957378.1:n.1677C=
NM_000365.6:c.669C= MANE Select NP_000356.1:p.Ser223=
NM_001258026.2:c.423C= NP_001244955.1:p.Ser141=