Canonical Allele Identifier: CA383713427
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870267T>C , CM000674.2:g.6870267T>C GRCh38
NC_000012.11:g.6979431T>C , CM000674.1:g.6979431T>C GRCh37
NC_000012.10:g.6849692T>C NCBI36
NG_011948.1:g.7848T>C
NG_013308.1:g.8091A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.634T>C MANE Select ENSP00000379933.4:p.Ser212Pro
ENST00000229270.8:c.745T>C ENSP00000229270.4:p.Ser249Pro
ENST00000396705.9:c.634T>C ENSP00000379933.4:p.Ser212Pro
ENST00000474253.1:n.123T>C
ENST00000488464.6:c.388T>C ENSP00000475620.1:p.Ser130Pro
ENST00000535434.5:c.388T>C ENSP00000443599.1:p.Ser130Pro
ENST00000613953.4:c.745T>C ENSP00000484435.1:p.Ser249Pro
NM_000365.5:c.634T>C NP_000356.1:p.Ser212Pro
NM_001159287.1:c.745T>C NP_001152759.1:p.Ser249Pro
NM_001258026.1:c.388T>C NP_001244955.1:p.Ser130Pro
XR_002957378.1:n.1642T>C
NM_000365.6:c.634T>C MANE Select NP_000356.1:p.Ser212Pro
NM_001258026.2:c.388T>C NP_001244955.1:p.Ser130Pro