Canonical Allele Identifier: CA478165057

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979242A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870078A>T , CM000674.2:g.6870078A>T	GRCh38
NC_000012.11:g.6979242A>T , CM000674.1:g.6979242A>T	GRCh37
NC_000012.10:g.6849503A>T	NCBI36
NG_011948.1:g.7659A>T
NG_013308.1:g.8280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.573A>T MANE Select	ENSP00000379933.4:p.Gly191=
ENST00000229270.8:c.684A>T	ENSP00000229270.4:p.Gly228=
ENST00000396705.9:c.573A>T	ENSP00000379933.4:p.Gly191=
ENST00000474253.1:n.62A>T
ENST00000482209.1:n.269A>T
ENST00000488464.6:c.327A>T	ENSP00000475620.1:p.Gly109=
ENST00000493987.5:c.327A>T	ENSP00000475364.1:p.Gly109=
ENST00000535434.5:c.327A>T	ENSP00000443599.1:p.Gly109=
ENST00000613953.4:c.684A>T	ENSP00000484435.1:p.Gly228=
NM_000365.5:c.573A>T	NP_000356.1:p.Gly191=
NM_001159287.1:c.684A>T	NP_001152759.1:p.Gly228=
NM_001258026.1:c.327A>T	NP_001244955.1:p.Gly109=
XR_002957378.1:n.1581A>T
NM_000365.6:c.573A>T MANE Select	NP_000356.1:p.Gly191=
NM_001258026.2:c.327A>T	NP_001244955.1:p.Gly109=