Canonical Allele Identifier: CA383713426

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979431T>A (hg19) ; chr12:g.6870267T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870267T>A , CM000674.2:g.6870267T>A	GRCh38
NC_000012.11:g.6979431T>A , CM000674.1:g.6979431T>A	GRCh37
NC_000012.10:g.6849692T>A	NCBI36
NG_011948.1:g.7848T>A
NG_013308.1:g.8091A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.634T>A MANE Select	ENSP00000379933.4:p.Ser212Thr
ENST00000229270.8:c.745T>A	ENSP00000229270.4:p.Ser249Thr
ENST00000396705.9:c.634T>A	ENSP00000379933.4:p.Ser212Thr
ENST00000474253.1:n.123T>A
ENST00000488464.6:c.388T>A	ENSP00000475620.1:p.Ser130Thr
ENST00000535434.5:c.388T>A	ENSP00000443599.1:p.Ser130Thr
ENST00000613953.4:c.745T>A	ENSP00000484435.1:p.Ser249Thr
NM_000365.5:c.634T>A	NP_000356.1:p.Ser212Thr
NM_001159287.1:c.745T>A	NP_001152759.1:p.Ser249Thr
NM_001258026.1:c.388T>A	NP_001244955.1:p.Ser130Thr
XR_002957378.1:n.1642T>A
NM_000365.6:c.634T>A MANE Select	NP_000356.1:p.Ser212Thr
NM_001258026.2:c.388T>A	NP_001244955.1:p.Ser130Thr