Canonical Allele Identifier: CA383713607

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979456A>C (hg19) ; chr12:g.6870292A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870292A>C , CM000674.2:g.6870292A>C	GRCh38
NC_000012.11:g.6979456A>C , CM000674.1:g.6979456A>C	GRCh37
NC_000012.10:g.6849717A>C	NCBI36
NG_011948.1:g.7873A>C
NG_013308.1:g.8066T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.659A>C MANE Select	ENSP00000379933.4:p.Glu220Ala
ENST00000229270.8:c.770A>C	ENSP00000229270.4:p.Glu257Ala
ENST00000396705.9:c.659A>C	ENSP00000379933.4:p.Glu220Ala
ENST00000474253.1:n.148A>C
ENST00000488464.6:c.413A>C	ENSP00000475620.1:p.Glu138Ala
ENST00000535434.5:c.413A>C	ENSP00000443599.1:p.Glu138Ala
ENST00000613953.4:c.770A>C	ENSP00000484435.1:p.Glu257Ala
NM_000365.5:c.659A>C	NP_000356.1:p.Glu220Ala
NM_001159287.1:c.770A>C	NP_001152759.1:p.Glu257Ala
NM_001258026.1:c.413A>C	NP_001244955.1:p.Glu138Ala
XR_002957378.1:n.1667A>C
NM_000365.6:c.659A>C MANE Select	NP_000356.1:p.Glu220Ala
NM_001258026.2:c.413A>C	NP_001244955.1:p.Glu138Ala