Canonical Allele Identifier: CA383713650

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979464A>C (hg19) ; chr12:g.6870300A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870300A>C , CM000674.2:g.6870300A>C	GRCh38
NC_000012.11:g.6979464A>C , CM000674.1:g.6979464A>C	GRCh37
NC_000012.10:g.6849725A>C	NCBI36
NG_011948.1:g.7881A>C
NG_013308.1:g.8058T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.667A>C MANE Select	ENSP00000379933.4:p.Ser223Arg
ENST00000229270.8:c.778A>C	ENSP00000229270.4:p.Ser260Arg
ENST00000396705.9:c.667A>C	ENSP00000379933.4:p.Ser223Arg
ENST00000474253.1:n.156A>C
ENST00000488464.6:c.421A>C	ENSP00000475620.1:p.Ser141Arg
ENST00000535434.5:c.421A>C	ENSP00000443599.1:p.Ser141Arg
ENST00000613953.4:c.778A>C	ENSP00000484435.1:p.Ser260Arg
NM_000365.5:c.667A>C	NP_000356.1:p.Ser223Arg
NM_001159287.1:c.778A>C	NP_001152759.1:p.Ser260Arg
NM_001258026.1:c.421A>C	NP_001244955.1:p.Ser141Arg
XR_002957378.1:n.1675A>C
NM_000365.6:c.667A>C MANE Select	NP_000356.1:p.Ser223Arg
NM_001258026.2:c.421A>C	NP_001244955.1:p.Ser141Arg