Canonical Allele Identifier: CA2014289800
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870615G= , CM000674.2:g.6870615G= GRCh38
NC_000012.11:g.6979779G= , CM000674.1:g.6979779G= GRCh37
NC_000012.10:g.6850040G= NCBI36
NG_011948.1:g.8196G=
NG_013308.1:g.7743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*232G= MANE Select ENSP00000379933.4:n.*232G=
ENST00000229270.8:c.*232G= ENSP00000229270.4:n.*232G=
ENST00000396705.9:c.*232G= ENSP00000379933.4:n.*232G=
ENST00000535434.5:c.*232G= ENSP00000443599.1:n.*232G=
ENST00000613953.4:c.*232G= ENSP00000484435.1:n.*232G=
NM_000365.5:c.*232G= NP_000356.1:n.*232G=
NM_001159287.1:c.*232G= NP_001152759.1:n.*232G=
NM_001258026.1:c.*232G= NP_001244955.1:n.*232G=
XR_002957378.1:n.1990G=
NM_000365.6:c.*232G= MANE Select NP_000356.1:n.*232G=
NM_001258026.2:c.*232G= NP_001244955.1:n.*232G=