Canonical Allele Identifier: CA383710199
Gene: TPI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6978338G>T (hg19) chr12:g.6869174G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869174G>T , CM000674.2:g.6869174G>T GRCh38
NC_000012.11:g.6978338G>T , CM000674.1:g.6978338G>T GRCh37
NC_000012.10:g.6848599G>T NCBI36
NG_011948.1:g.6755G>T
NG_013308.1:g.9184C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.315G>T MANE Select ENSP00000379933.4:p.Glu105Asp
ENST00000229270.8:c.426G>T ENSP00000229270.4:p.Glu142Asp
ENST00000396705.9:c.315G>T ENSP00000379933.4:p.Glu105Asp
ENST00000462761.5:c.69G>T ENSP00000475184.1:p.Glu23Asp
ENST00000488464.6:c.69G>T ENSP00000475620.1:p.Glu23Asp
ENST00000493987.5:c.69G>T ENSP00000475364.1:p.Glu23Asp
ENST00000495834.1:c.69G>T ENSP00000475829.1:p.Glu23Asp
ENST00000535434.5:c.69G>T ENSP00000443599.1:p.Glu23Asp
ENST00000613953.4:c.426G>T ENSP00000484435.1:p.Glu142Asp
NM_000365.5:c.315G>T NP_000356.1:p.Glu105Asp
NM_001159287.1:c.426G>T NP_001152759.1:p.Glu142Asp
NM_001258026.1:c.69G>T NP_001244955.1:p.Glu23Asp
XR_002957378.1:n.1048G>T
NM_000365.6:c.315G>T MANE Select NP_000356.1:p.Glu105Asp
NM_001258026.2:c.69G>T NP_001244955.1:p.Glu23Asp
Search 100 bp 5'
Search 100 bp 3'