Canonical Allele Identifier: CA2617354838

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870155-C-CGGCTGAGGTGGAGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870164_6870178dup , CM000674.2:g.6870164_6870178dup	GRCh38
NC_000012.11:g.6979328_6979342dup , CM000674.1:g.6979328_6979342dup	GRCh37
NC_000012.10:g.6849589_6849603dup	NCBI36
NG_011948.1:g.7745_7759dup
NG_013308.1:g.8188_8202dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.631+28_631+42dup MANE Select	ENSP00000379933.4:n.631+28_631+42dup
ENST00000229270.8:c.742+28_742+42dup	ENSP00000229270.4:n.742+28_742+42dup
ENST00000396705.9:c.631+28_631+42dup	ENSP00000379933.4:n.631+28_631+42dup
ENST00000474253.1:n.120+28_120+42dup
ENST00000488464.6:c.385+28_385+42dup	ENSP00000475620.1:n.385+28_385+42dup
ENST00000535434.5:c.385+28_385+42dup	ENSP00000443599.1:n.385+28_385+42dup
ENST00000613953.4:c.742+28_742+42dup	ENSP00000484435.1:n.742+28_742+42dup
NM_000365.5:c.631+28_631+42dup	NP_000356.1:n.631+28_631+42dup
NM_001159287.1:c.742+28_742+42dup	NP_001152759.1:n.742+28_742+42dup
NM_001258026.1:c.385+28_385+42dup	NP_001244955.1:n.385+28_385+42dup
XR_002957378.1:n.1639+28_1639+42dup
NM_000365.6:c.631+28_631+42dup MANE Select	NP_000356.1:n.631+28_631+42dup
NM_001258026.2:c.385+28_385+42dup	NP_001244955.1:n.385+28_385+42dup