Canonical Allele Identifier: CA383714263

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979528T>G (hg19) ; chr12:g.6870364T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870364T>G , CM000674.2:g.6870364T>G	GRCh38
NC_000012.11:g.6979528T>G , CM000674.1:g.6979528T>G	GRCh37
NC_000012.10:g.6849789T>G	NCBI36
NG_011948.1:g.7945T>G
NG_013308.1:g.7994A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.731T>G MANE Select	ENSP00000379933.4:p.Ile244Ser
ENST00000229270.8:c.842T>G	ENSP00000229270.4:p.Ile281Ser
ENST00000396705.9:c.731T>G	ENSP00000379933.4:p.Ile244Ser
ENST00000474253.1:n.220T>G
ENST00000488464.6:c.485T>G	ENSP00000475620.1:p.Ile162Ser
ENST00000535434.5:c.485T>G	ENSP00000443599.1:p.Ile162Ser
ENST00000613953.4:c.842T>G	ENSP00000484435.1:p.Ile281Ser
NM_000365.5:c.731T>G	NP_000356.1:p.Ile244Ser
NM_001159287.1:c.842T>G	NP_001152759.1:p.Ile281Ser
NM_001258026.1:c.485T>G	NP_001244955.1:p.Ile162Ser
XR_002957378.1:n.1739T>G
NM_000365.6:c.731T>G MANE Select	NP_000356.1:p.Ile244Ser
NM_001258026.2:c.485T>G	NP_001244955.1:p.Ile162Ser