Canonical Allele Identifier: CA383713793

Gene: TPI1

Linked Data

• dbSNP Id: rs1396813353
• gnomAD v3: 12-6870312-G-A
• gnomAD v4: 12-6870312-G-A
• MyVariant Identifiers: chr12:g.6979476G>A (hg19) ; chr12:g.6870312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870312G>A , CM000674.2:g.6870312G>A	GRCh38
NC_000012.11:g.6979476G>A , CM000674.1:g.6979476G>A	GRCh37
NC_000012.10:g.6849737G>A	NCBI36
NG_011948.1:g.7893G>A
NG_013308.1:g.8046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.679G>A MANE Select	ENSP00000379933.4:p.Val227Met
ENST00000229270.8:c.790G>A	ENSP00000229270.4:p.Val264Met
ENST00000396705.9:c.679G>A	ENSP00000379933.4:p.Val227Met
ENST00000474253.1:n.168G>A
ENST00000488464.6:c.433G>A	ENSP00000475620.1:p.Val145Met
ENST00000535434.5:c.433G>A	ENSP00000443599.1:p.Val145Met
ENST00000613953.4:c.790G>A	ENSP00000484435.1:p.Val264Met
NM_000365.5:c.679G>A	NP_000356.1:p.Val227Met
NM_001159287.1:c.790G>A	NP_001152759.1:p.Val264Met
NM_001258026.1:c.433G>A	NP_001244955.1:p.Val145Met
XR_002957378.1:n.1687G>A
NM_000365.6:c.679G>A MANE Select	NP_000356.1:p.Val227Met
NM_001258026.2:c.433G>A	NP_001244955.1:p.Val145Met