Canonical Allele Identifier: CA383713812

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979479G>C (hg19) ; chr12:g.6870315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870315G>C , CM000674.2:g.6870315G>C	GRCh38
NC_000012.11:g.6979479G>C , CM000674.1:g.6979479G>C	GRCh37
NC_000012.10:g.6849740G>C	NCBI36
NG_011948.1:g.7896G>C
NG_013308.1:g.8043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.682G>C MANE Select	ENSP00000379933.4:p.Asp228His
ENST00000229270.8:c.793G>C	ENSP00000229270.4:p.Asp265His
ENST00000396705.9:c.682G>C	ENSP00000379933.4:p.Asp228His
ENST00000474253.1:n.171G>C
ENST00000488464.6:c.436G>C	ENSP00000475620.1:p.Asp146His
ENST00000535434.5:c.436G>C	ENSP00000443599.1:p.Asp146His
ENST00000613953.4:c.793G>C	ENSP00000484435.1:p.Asp265His
NM_000365.5:c.682G>C	NP_000356.1:p.Asp228His
NM_001159287.1:c.793G>C	NP_001152759.1:p.Asp265His
NM_001258026.1:c.436G>C	NP_001244955.1:p.Asp146His
XR_002957378.1:n.1690G>C
NM_000365.6:c.682G>C MANE Select	NP_000356.1:p.Asp228His
NM_001258026.2:c.436G>C	NP_001244955.1:p.Asp146His