Canonical Allele Identifier: CA383714060

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979513C>G (hg19) ; chr12:g.6870349C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870349C>G , CM000674.2:g.6870349C>G	GRCh38
NC_000012.11:g.6979513C>G , CM000674.1:g.6979513C>G	GRCh37
NC_000012.10:g.6849774C>G	NCBI36
NG_011948.1:g.7930C>G
NG_013308.1:g.8009G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.716C>G MANE Select	ENSP00000379933.4:p.Pro239Arg
ENST00000229270.8:c.827C>G	ENSP00000229270.4:p.Pro276Arg
ENST00000396705.9:c.716C>G	ENSP00000379933.4:p.Pro239Arg
ENST00000474253.1:n.205C>G
ENST00000488464.6:c.470C>G	ENSP00000475620.1:p.Pro157Arg
ENST00000535434.5:c.470C>G	ENSP00000443599.1:p.Pro157Arg
ENST00000613953.4:c.827C>G	ENSP00000484435.1:p.Pro276Arg
NM_000365.5:c.716C>G	NP_000356.1:p.Pro239Arg
NM_001159287.1:c.827C>G	NP_001152759.1:p.Pro276Arg
NM_001258026.1:c.470C>G	NP_001244955.1:p.Pro157Arg
XR_002957378.1:n.1724C>G
NM_000365.6:c.716C>G MANE Select	NP_000356.1:p.Pro239Arg
NM_001258026.2:c.470C>G	NP_001244955.1:p.Pro157Arg