Canonical Allele Identifier: CA383712687

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979213G>A (hg19) ; chr12:g.6870049G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870049G>A , CM000674.2:g.6870049G>A	GRCh38
NC_000012.11:g.6979213G>A , CM000674.1:g.6979213G>A	GRCh37
NC_000012.10:g.6849474G>A	NCBI36
NG_011948.1:g.7630G>A
NG_013308.1:g.8309C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.544G>A MANE Select	ENSP00000379933.4:p.Ala182Thr
ENST00000229270.8:c.655G>A	ENSP00000229270.4:p.Ala219Thr
ENST00000396705.9:c.544G>A	ENSP00000379933.4:p.Ala182Thr
ENST00000474253.1:n.33G>A
ENST00000482209.1:n.240G>A
ENST00000488464.6:c.298G>A	ENSP00000475620.1:p.Ala100Thr
ENST00000493987.5:c.298G>A	ENSP00000475364.1:p.Ala100Thr
ENST00000535434.5:c.298G>A	ENSP00000443599.1:p.Ala100Thr
ENST00000613953.4:c.655G>A	ENSP00000484435.1:p.Ala219Thr
NM_000365.5:c.544G>A	NP_000356.1:p.Ala182Thr
NM_001159287.1:c.655G>A	NP_001152759.1:p.Ala219Thr
NM_001258026.1:c.298G>A	NP_001244955.1:p.Ala100Thr
XR_002957378.1:n.1552G>A
NM_000365.6:c.544G>A MANE Select	NP_000356.1:p.Ala182Thr
NM_001258026.2:c.298G>A	NP_001244955.1:p.Ala100Thr