Canonical Allele Identifier: CA2014289529

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870092A= , CM000674.2:g.6870092A=	GRCh38
NC_000012.11:g.6979256A= , CM000674.1:g.6979256A=	GRCh37
NC_000012.10:g.6849517A=	NCBI36
NG_011948.1:g.7673A=
NG_013308.1:g.8266T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.587A= MANE Select	ENSP00000379933.4:p.Asn196=
ENST00000229270.8:c.698A=	ENSP00000229270.4:p.Asn233=
ENST00000396705.9:c.587A=	ENSP00000379933.4:p.Asn196=
ENST00000474253.1:n.76A=
ENST00000482209.1:n.283A=
ENST00000488464.6:c.341A=	ENSP00000475620.1:p.Asn114=
ENST00000535434.5:c.341A=	ENSP00000443599.1:p.Asn114=
ENST00000613953.4:c.698A=	ENSP00000484435.1:p.Asn233=
NM_000365.5:c.587A=	NP_000356.1:p.Asn196=
NM_001159287.1:c.698A=	NP_001152759.1:p.Asn233=
NM_001258026.1:c.341A=	NP_001244955.1:p.Asn114=
XR_002957378.1:n.1595A=
NM_000365.6:c.587A= MANE Select	NP_000356.1:p.Asn196=
NM_001258026.2:c.341A=	NP_001244955.1:p.Asn114=