Canonical Allele Identifier: CA383714313

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979533A>G (hg19) ; chr12:g.6870369A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870369A>G , CM000674.2:g.6870369A>G	GRCh38
NC_000012.11:g.6979533A>G , CM000674.1:g.6979533A>G	GRCh37
NC_000012.10:g.6849794A>G	NCBI36
NG_011948.1:g.7950A>G
NG_013308.1:g.7989T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.736A>G MANE Select	ENSP00000379933.4:p.Asn246Asp
ENST00000229270.8:c.847A>G	ENSP00000229270.4:p.Asn283Asp
ENST00000396705.9:c.736A>G	ENSP00000379933.4:p.Asn246Asp
ENST00000474253.1:n.225A>G
ENST00000488464.6:c.490A>G	ENSP00000475620.1:p.Asn164Asp
ENST00000535434.5:c.490A>G	ENSP00000443599.1:p.Asn164Asp
ENST00000613953.4:c.847A>G	ENSP00000484435.1:p.Asn283Asp
NM_000365.5:c.736A>G	NP_000356.1:p.Asn246Asp
NM_001159287.1:c.847A>G	NP_001152759.1:p.Asn283Asp
NM_001258026.1:c.490A>G	NP_001244955.1:p.Asn164Asp
XR_002957378.1:n.1744A>G
NM_000365.6:c.736A>G MANE Select	NP_000356.1:p.Asn246Asp
NM_001258026.2:c.490A>G	NP_001244955.1:p.Asn164Asp