Canonical Allele Identifier: CA478165893

Gene: TPI1

Linked Data

• dbSNP Id: rs1365888129
• gnomAD v3: 12-6870380-A-G
• gnomAD v4: 12-6870380-A-G
• MyVariant Identifiers: chr12:g.6979544A>G (hg19) ; chr12:g.6870380A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870380A>G , CM000674.2:g.6870380A>G	GRCh38
NC_000012.11:g.6979544A>G , CM000674.1:g.6979544A>G	GRCh37
NC_000012.10:g.6849805A>G	NCBI36
NG_011948.1:g.7961A>G
NG_013308.1:g.7978T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.747A>G MANE Select	ENSP00000379933.4:p.Gln249=
ENST00000229270.8:c.858A>G	ENSP00000229270.4:p.Gln286=
ENST00000396705.9:c.747A>G	ENSP00000379933.4:p.Gln249=
ENST00000474253.1:n.236A>G
ENST00000488464.6:c.501A>G	ENSP00000475620.1:p.Gln167=
ENST00000535434.5:c.501A>G	ENSP00000443599.1:p.Gln167=
ENST00000613953.4:c.858A>G	ENSP00000484435.1:p.Gln286=
NM_000365.5:c.747A>G	NP_000356.1:p.Gln249=
NM_001159287.1:c.858A>G	NP_001152759.1:p.Gln286=
NM_001258026.1:c.501A>G	NP_001244955.1:p.Gln167=
XR_002957378.1:n.1755A>G
NM_000365.6:c.747A>G MANE Select	NP_000356.1:p.Gln249=
NM_001258026.2:c.501A>G	NP_001244955.1:p.Gln167=