Canonical Allele Identifier: CA383713643

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979462C>G (hg19) ; chr12:g.6870298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870298C>G , CM000674.2:g.6870298C>G	GRCh38
NC_000012.11:g.6979462C>G , CM000674.1:g.6979462C>G	GRCh37
NC_000012.10:g.6849723C>G	NCBI36
NG_011948.1:g.7879C>G
NG_013308.1:g.8060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.665C>G MANE Select	ENSP00000379933.4:p.Ala222Gly
ENST00000229270.8:c.776C>G	ENSP00000229270.4:p.Ala259Gly
ENST00000396705.9:c.665C>G	ENSP00000379933.4:p.Ala222Gly
ENST00000474253.1:n.154C>G
ENST00000488464.6:c.419C>G	ENSP00000475620.1:p.Ala140Gly
ENST00000535434.5:c.419C>G	ENSP00000443599.1:p.Ala140Gly
ENST00000613953.4:c.776C>G	ENSP00000484435.1:p.Ala259Gly
NM_000365.5:c.665C>G	NP_000356.1:p.Ala222Gly
NM_001159287.1:c.776C>G	NP_001152759.1:p.Ala259Gly
NM_001258026.1:c.419C>G	NP_001244955.1:p.Ala140Gly
XR_002957378.1:n.1673C>G
NM_000365.6:c.665C>G MANE Select	NP_000356.1:p.Ala222Gly
NM_001258026.2:c.419C>G	NP_001244955.1:p.Ala140Gly