Canonical Allele Identifier: CA6418755
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6867524A>G , CM000674.2:g.6867524A>G GRCh38
NC_000012.11:g.6976688A>G , CM000674.1:g.6976688A>G GRCh37
NC_000012.10:g.6846949A>G NCBI36
NG_011948.1:g.5105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229270.8:c.69A>G ENSP00000229270.4:p.Arg23=
ENST00000613953.4:c.69A>G ENSP00000484435.1:p.Arg23=
NM_001159287.1:c.69A>G NP_001152759.1:p.Arg23=
XR_002957378.1:n.691A>G