Canonical Allele Identifier: CA383713780

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979474A>T (hg19) ; chr12:g.6870310A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870310A>T , CM000674.2:g.6870310A>T	GRCh38
NC_000012.11:g.6979474A>T , CM000674.1:g.6979474A>T	GRCh37
NC_000012.10:g.6849735A>T	NCBI36
NG_011948.1:g.7891A>T
NG_013308.1:g.8048T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.677A>T MANE Select	ENSP00000379933.4:p.Asp226Val
ENST00000229270.8:c.788A>T	ENSP00000229270.4:p.Asp263Val
ENST00000396705.9:c.677A>T	ENSP00000379933.4:p.Asp226Val
ENST00000474253.1:n.166A>T
ENST00000488464.6:c.431A>T	ENSP00000475620.1:p.Asp144Val
ENST00000535434.5:c.431A>T	ENSP00000443599.1:p.Asp144Val
ENST00000613953.4:c.788A>T	ENSP00000484435.1:p.Asp263Val
NM_000365.5:c.677A>T	NP_000356.1:p.Asp226Val
NM_001159287.1:c.788A>T	NP_001152759.1:p.Asp263Val
NM_001258026.1:c.431A>T	NP_001244955.1:p.Asp144Val
XR_002957378.1:n.1685A>T
NM_000365.6:c.677A>T MANE Select	NP_000356.1:p.Asp226Val
NM_001258026.2:c.431A>T	NP_001244955.1:p.Asp144Val