Canonical Allele Identifier: CA691293184

Gene: TPI1

Linked Data

• dbSNP Id: rs1415063595
• gnomAD v3: 12-6870023-T-A
• gnomAD v4: 12-6870023-T-A
• MyVariant Identifiers: chr12:g.6870023T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870023T>A , CM000674.2:g.6870023T>A	GRCh38
NC_000012.11:g.6979187T>A , CM000674.1:g.6979187T>A	GRCh37
NC_000012.10:g.6849448T>A	NCBI36
NG_011948.1:g.7604T>A
NG_013308.1:g.8335A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.544-26T>A MANE Select	ENSP00000379933.4:n.544-26T>A
ENST00000229270.8:c.655-26T>A	ENSP00000229270.4:n.655-26T>A
ENST00000396705.9:c.544-26T>A	ENSP00000379933.4:n.544-26T>A
ENST00000474253.1:n.7T>A
ENST00000482209.1:n.227-13T>A
ENST00000488464.6:c.298-26T>A	ENSP00000475620.1:n.298-26T>A
ENST00000493987.5:c.298-26T>A	ENSP00000475364.1:n.298-26T>A
ENST00000535434.5:c.298-26T>A	ENSP00000443599.1:n.298-26T>A
ENST00000613953.4:c.655-26T>A	ENSP00000484435.1:n.655-26T>A
NM_000365.5:c.544-26T>A	NP_000356.1:n.544-26T>A
NM_001159287.1:c.655-26T>A	NP_001152759.1:n.655-26T>A
NM_001258026.1:c.298-26T>A	NP_001244955.1:n.298-26T>A
XR_002957378.1:n.1526T>A
NM_000365.6:c.544-26T>A MANE Select	NP_000356.1:n.544-26T>A
NM_001258026.2:c.298-26T>A	NP_001244955.1:n.298-26T>A