Canonical Allele Identifier: CA603133024

Gene: TPI1

Linked Data

• dbSNP Id: rs1357359928
• gnomAD v2: 12-6979688-T-A
• gnomAD v4: 12-6870524-T-A
• MyVariant Identifiers: chr12:g.6979688T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870524T>A , CM000674.2:g.6870524T>A	GRCh38
NC_000012.11:g.6979688T>A , CM000674.1:g.6979688T>A	GRCh37
NC_000012.10:g.6849949T>A	NCBI36
NG_011948.1:g.8105T>A
NG_013308.1:g.7834A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*141T>A MANE Select	ENSP00000379933.4:n.*141T>A
ENST00000229270.8:c.*141T>A	ENSP00000229270.4:n.*141T>A
ENST00000396705.9:c.*141T>A	ENSP00000379933.4:n.*141T>A
ENST00000474253.1:n.380T>A
ENST00000535434.5:c.*141T>A	ENSP00000443599.1:n.*141T>A
ENST00000613953.4:c.*141T>A	ENSP00000484435.1:n.*141T>A
NM_000365.5:c.*141T>A	NP_000356.1:n.*141T>A
NM_001159287.1:c.*141T>A	NP_001152759.1:n.*141T>A
NM_001258026.1:c.*141T>A	NP_001244955.1:n.*141T>A
XR_002957378.1:n.1899T>A
NM_000365.6:c.*141T>A MANE Select	NP_000356.1:n.*141T>A
NM_001258026.2:c.*141T>A	NP_001244955.1:n.*141T>A