Canonical Allele Identifier: CA603133032

Gene: TPI1

Linked Data

• dbSNP Id: rs1565538901
• gnomAD v2: 12-6979746-C-CTA
• gnomAD v4: 12-6870582-C-CTA
• MyVariant Identifiers: chr12:g.6979746_6979747insTA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870585_6870586dup , CM000674.2:g.6870585_6870586dup	GRCh38
NC_000012.11:g.6979749_6979750dup , CM000674.1:g.6979749_6979750dup	GRCh37
NC_000012.10:g.6850010_6850011dup	NCBI36
NG_011948.1:g.8166_8167dup
NG_013308.1:g.7774_7775dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*202_*203dup MANE Select	ENSP00000379933.4:n.*202_*203dup
ENST00000229270.8:c.*202_*203dup	ENSP00000229270.4:n.*202_*203dup
ENST00000396705.9:c.*202_*203dup	ENSP00000379933.4:n.*202_*203dup
ENST00000535434.5:c.*202_*203dup	ENSP00000443599.1:n.*202_*203dup
ENST00000613953.4:c.*202_*203dup	ENSP00000484435.1:n.*202_*203dup
NM_000365.5:c.*202_*203dup	NP_000356.1:n.*202_*203dup
NM_001159287.1:c.*202_*203dup	NP_001152759.1:n.*202_*203dup
NM_001258026.1:c.*202_*203dup	NP_001244955.1:n.*202_*203dup
XR_002957378.1:n.1960_1961dup
NM_000365.6:c.*202_*203dup MANE Select	NP_000356.1:n.*202_*203dup
NM_001258026.2:c.*202_*203dup	NP_001244955.1:n.*202_*203dup