Canonical Allele Identifier: CA2014289622
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870265G= , CM000674.2:g.6870265G= GRCh38
NC_000012.11:g.6979429G= , CM000674.1:g.6979429G= GRCh37
NC_000012.10:g.6849690G= NCBI36
NG_011948.1:g.7846G=
NG_013308.1:g.8093C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.632G= MANE Select ENSP00000379933.4:p.Gly211=
ENST00000229270.8:c.743G= ENSP00000229270.4:p.Gly248=
ENST00000396705.9:c.632G= ENSP00000379933.4:p.Gly211=
ENST00000474253.1:n.121G=
ENST00000488464.6:c.386G= ENSP00000475620.1:p.Gly129=
ENST00000535434.5:c.386G= ENSP00000443599.1:p.Gly129=
ENST00000613953.4:c.743G= ENSP00000484435.1:p.Gly248=
NM_000365.5:c.632G= NP_000356.1:p.Gly211=
NM_001159287.1:c.743G= NP_001152759.1:p.Gly248=
NM_001258026.1:c.386G= NP_001244955.1:p.Gly129=
XR_002957378.1:n.1640G=
NM_000365.6:c.632G= MANE Select NP_000356.1:p.Gly211=
NM_001258026.2:c.386G= NP_001244955.1:p.Gly129=