Canonical Allele Identifier: CA2014289623
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870269T= , CM000674.2:g.6870269T= GRCh38
NC_000012.11:g.6979433T= , CM000674.1:g.6979433T= GRCh37
NC_000012.10:g.6849694T= NCBI36
NG_011948.1:g.7850T=
NG_013308.1:g.8089A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.636T= MANE Select ENSP00000379933.4:p.Ser212=
ENST00000229270.8:c.747T= ENSP00000229270.4:p.Ser249=
ENST00000396705.9:c.636T= ENSP00000379933.4:p.Ser212=
ENST00000474253.1:n.125T=
ENST00000488464.6:c.390T= ENSP00000475620.1:p.Ser130=
ENST00000535434.5:c.390T= ENSP00000443599.1:p.Ser130=
ENST00000613953.4:c.747T= ENSP00000484435.1:p.Ser249=
NM_000365.5:c.636T= NP_000356.1:p.Ser212=
NM_001159287.1:c.747T= NP_001152759.1:p.Ser249=
NM_001258026.1:c.390T= NP_001244955.1:p.Ser130=
XR_002957378.1:n.1644T=
NM_000365.6:c.636T= MANE Select NP_000356.1:p.Ser212=
NM_001258026.2:c.390T= NP_001244955.1:p.Ser130=