Canonical Allele Identifier: CA383713279

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979297G>T (hg19) ; chr12:g.6870133G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870133G>T , CM000674.2:g.6870133G>T	GRCh38
NC_000012.11:g.6979297G>T , CM000674.1:g.6979297G>T	GRCh37
NC_000012.10:g.6849558G>T	NCBI36
NG_011948.1:g.7714G>T
NG_013308.1:g.8225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.628G>T MANE Select	ENSP00000379933.4:p.Gly210Ter
ENST00000229270.8:c.739G>T	ENSP00000229270.4:p.Gly247Ter
ENST00000396705.9:c.628G>T	ENSP00000379933.4:p.Gly210Ter
ENST00000474253.1:n.117G>T
ENST00000482209.1:n.324G>T
ENST00000488464.6:c.382G>T	ENSP00000475620.1:p.Gly128Ter
ENST00000535434.5:c.382G>T	ENSP00000443599.1:p.Gly128Ter
ENST00000613953.4:c.739G>T	ENSP00000484435.1:p.Gly247Ter
NM_000365.5:c.628G>T	NP_000356.1:p.Gly210Ter
NM_001159287.1:c.739G>T	NP_001152759.1:p.Gly247Ter
NM_001258026.1:c.382G>T	NP_001244955.1:p.Gly128Ter
XR_002957378.1:n.1636G>T
NM_000365.6:c.628G>T MANE Select	NP_000356.1:p.Gly210Ter
NM_001258026.2:c.382G>T	NP_001244955.1:p.Gly128Ter