Canonical Allele Identifier: CA2014289699

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870431G= , CM000674.2:g.6870431G=	GRCh38
NC_000012.11:g.6979595G= , CM000674.1:g.6979595G=	GRCh37
NC_000012.10:g.6849856G=	NCBI36
NG_011948.1:g.8012G=
NG_013308.1:g.7927C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*48G= MANE Select	ENSP00000379933.4:n.*48G=
ENST00000229270.8:c.*48G=	ENSP00000229270.4:n.*48G=
ENST00000396705.9:c.*48G=	ENSP00000379933.4:n.*48G=
ENST00000474253.1:n.287G=
ENST00000535434.5:c.*48G=	ENSP00000443599.1:n.*48G=
ENST00000613953.4:c.*48G=	ENSP00000484435.1:n.*48G=
NM_000365.5:c.*48G=	NP_000356.1:n.*48G=
NM_001159287.1:c.*48G=	NP_001152759.1:n.*48G=
NM_001258026.1:c.*48G=	NP_001244955.1:n.*48G=
XR_002957378.1:n.1806G=
NM_000365.6:c.*48G= MANE Select	NP_000356.1:n.*48G=
NM_001258026.2:c.*48G=	NP_001244955.1:n.*48G=