Canonical Allele Identifier: CA478165866

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979523G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870359G>T , CM000674.2:g.6870359G>T	GRCh38
NC_000012.11:g.6979523G>T , CM000674.1:g.6979523G>T	GRCh37
NC_000012.10:g.6849784G>T	NCBI36
NG_011948.1:g.7940G>T
NG_013308.1:g.7999C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.726G>T MANE Select	ENSP00000379933.4:p.Val242=
ENST00000229270.8:c.837G>T	ENSP00000229270.4:p.Val279=
ENST00000396705.9:c.726G>T	ENSP00000379933.4:p.Val242=
ENST00000474253.1:n.215G>T
ENST00000488464.6:c.480G>T	ENSP00000475620.1:p.Val160=
ENST00000535434.5:c.480G>T	ENSP00000443599.1:p.Val160=
ENST00000613953.4:c.837G>T	ENSP00000484435.1:p.Val279=
NM_000365.5:c.726G>T	NP_000356.1:p.Val242=
NM_001159287.1:c.837G>T	NP_001152759.1:p.Val279=
NM_001258026.1:c.480G>T	NP_001244955.1:p.Val160=
XR_002957378.1:n.1734G>T
NM_000365.6:c.726G>T MANE Select	NP_000356.1:p.Val242=
NM_001258026.2:c.480G>T	NP_001244955.1:p.Val160=