Canonical Allele Identifier: CA2014289512

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870053A= , CM000674.2:g.6870053A=	GRCh38
NC_000012.11:g.6979217A= , CM000674.1:g.6979217A=	GRCh37
NC_000012.10:g.6849478A=	NCBI36
NG_011948.1:g.7634A=
NG_013308.1:g.8305T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.548A= MANE Select	ENSP00000379933.4:p.Gln183=
ENST00000229270.8:c.659A=	ENSP00000229270.4:p.Gln220=
ENST00000396705.9:c.548A=	ENSP00000379933.4:p.Gln183=
ENST00000474253.1:n.37A=
ENST00000482209.1:n.244A=
ENST00000488464.6:c.302A=	ENSP00000475620.1:p.Gln101=
ENST00000493987.5:c.302A=	ENSP00000475364.1:p.Gln101=
ENST00000535434.5:c.302A=	ENSP00000443599.1:p.Gln101=
ENST00000613953.4:c.659A=	ENSP00000484435.1:p.Gln220=
NM_000365.5:c.548A=	NP_000356.1:p.Gln183=
NM_001159287.1:c.659A=	NP_001152759.1:p.Gln220=
NM_001258026.1:c.302A=	NP_001244955.1:p.Gln101=
XR_002957378.1:n.1556A=
NM_000365.6:c.548A= MANE Select	NP_000356.1:p.Gln183=
NM_001258026.2:c.302A=	NP_001244955.1:p.Gln101=