Canonical Allele Identifier: CA478163781

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6976688A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6867524A>T , CM000674.2:g.6867524A>T	GRCh38
NC_000012.11:g.6976688A>T , CM000674.1:g.6976688A>T	GRCh37
NC_000012.10:g.6846949A>T	NCBI36
NG_011948.1:g.5105A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229270.8:c.69A>T	ENSP00000229270.4:p.Arg23=
ENST00000613953.4:c.69A>T	ENSP00000484435.1:p.Arg23=
NM_001159287.1:c.69A>T	NP_001152759.1:p.Arg23=
XR_002957378.1:n.691A>T