Canonical Allele Identifier: CA383712915

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979253C>G (hg19) ; chr12:g.6870089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870089C>G , CM000674.2:g.6870089C>G	GRCh38
NC_000012.11:g.6979253C>G , CM000674.1:g.6979253C>G	GRCh37
NC_000012.10:g.6849514C>G	NCBI36
NG_011948.1:g.7670C>G
NG_013308.1:g.8269G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.584C>G MANE Select	ENSP00000379933.4:p.Ser195Cys
ENST00000229270.8:c.695C>G	ENSP00000229270.4:p.Ser232Cys
ENST00000396705.9:c.584C>G	ENSP00000379933.4:p.Ser195Cys
ENST00000474253.1:n.73C>G
ENST00000482209.1:n.280C>G
ENST00000488464.6:c.338C>G	ENSP00000475620.1:p.Ser113Cys
ENST00000493987.5:c.338C>G	ENSP00000475364.1:p.Ser113Cys
ENST00000535434.5:c.338C>G	ENSP00000443599.1:p.Ser113Cys
ENST00000613953.4:c.695C>G	ENSP00000484435.1:p.Ser232Cys
NM_000365.5:c.584C>G	NP_000356.1:p.Ser195Cys
NM_001159287.1:c.695C>G	NP_001152759.1:p.Ser232Cys
NM_001258026.1:c.338C>G	NP_001244955.1:p.Ser113Cys
XR_002957378.1:n.1592C>G
NM_000365.6:c.584C>G MANE Select	NP_000356.1:p.Ser195Cys
NM_001258026.2:c.338C>G	NP_001244955.1:p.Ser113Cys