Canonical Allele Identifier: CA383714293

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979531T>C (hg19) ; chr12:g.6870367T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870367T>C , CM000674.2:g.6870367T>C	GRCh38
NC_000012.11:g.6979531T>C , CM000674.1:g.6979531T>C	GRCh37
NC_000012.10:g.6849792T>C	NCBI36
NG_011948.1:g.7948T>C
NG_013308.1:g.7991A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.734T>C MANE Select	ENSP00000379933.4:p.Ile245Thr
ENST00000229270.8:c.845T>C	ENSP00000229270.4:p.Ile282Thr
ENST00000396705.9:c.734T>C	ENSP00000379933.4:p.Ile245Thr
ENST00000474253.1:n.223T>C
ENST00000488464.6:c.488T>C	ENSP00000475620.1:p.Ile163Thr
ENST00000535434.5:c.488T>C	ENSP00000443599.1:p.Ile163Thr
ENST00000613953.4:c.845T>C	ENSP00000484435.1:p.Ile282Thr
NM_000365.5:c.734T>C	NP_000356.1:p.Ile245Thr
NM_001159287.1:c.845T>C	NP_001152759.1:p.Ile282Thr
NM_001258026.1:c.488T>C	NP_001244955.1:p.Ile163Thr
XR_002957378.1:n.1742T>C
NM_000365.6:c.734T>C MANE Select	NP_000356.1:p.Ile245Thr
NM_001258026.2:c.488T>C	NP_001244955.1:p.Ile163Thr