Canonical Allele Identifier: CA2014289567

Gene: TPI1

Linked Data

• dbSNP Id: rs1591618123

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870164T>G , CM000674.2:g.6870164T>G	GRCh38
NC_000012.11:g.6979328T>G , CM000674.1:g.6979328T>G	GRCh37
NC_000012.10:g.6849589T>G	NCBI36
NG_011948.1:g.7745T>G
NG_013308.1:g.8194A>C

Transcript Alleles

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