Canonical Allele Identifier: CA478164549

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6978038T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6868874T>C , CM000674.2:g.6868874T>C	GRCh38
NC_000012.11:g.6978038T>C , CM000674.1:g.6978038T>C	GRCh37
NC_000012.10:g.6848299T>C	NCBI36
NG_011948.1:g.6455T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.126T>C MANE Select	ENSP00000379933.4:p.Cys42=
ENST00000229270.8:c.237T>C	ENSP00000229270.4:p.Cys79=
ENST00000396705.9:c.126T>C	ENSP00000379933.4:p.Cys42=
ENST00000462761.5:c.-121T>C	ENSP00000475184.1:n.-121T>C
ENST00000488464.6:c.-121T>C	ENSP00000475620.1:n.-121T>C
ENST00000493987.5:c.-121T>C	ENSP00000475364.1:n.-121T>C
ENST00000495834.1:c.-121T>C	ENSP00000475829.1:n.-121T>C
ENST00000535434.5:c.-121T>C	ENSP00000443599.1:n.-121T>C
ENST00000613953.4:c.237T>C	ENSP00000484435.1:p.Cys79=
NM_000365.5:c.126T>C	NP_000356.1:p.Cys42=
NM_001159287.1:c.237T>C	NP_001152759.1:p.Cys79=
NM_001258026.1:c.-121T>C	NP_001244955.1:n.-121T>C
XR_002957378.1:n.859T>C
NM_000365.6:c.126T>C MANE Select	NP_000356.1:p.Cys42=
NM_001258026.2:c.-121T>C	NP_001244955.1:n.-121T>C