Canonical Allele Identifier: CA383712465

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6978909G>C (hg19) ; chr12:g.6869745G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6869745G>C , CM000674.2:g.6869745G>C	GRCh38
NC_000012.11:g.6978909G>C , CM000674.1:g.6978909G>C	GRCh37
NC_000012.10:g.6849170G>C	NCBI36
NG_011948.1:g.7326G>C
NG_013308.1:g.8613C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.515G>C MANE Select	ENSP00000379933.4:p.Gly172Ala
ENST00000229270.8:c.626G>C	ENSP00000229270.4:p.Gly209Ala
ENST00000396705.9:c.515G>C	ENSP00000379933.4:p.Gly172Ala
ENST00000482209.1:n.198G>C
ENST00000488464.6:c.269G>C	ENSP00000475620.1:p.Gly90Ala
ENST00000493987.5:c.269G>C	ENSP00000475364.1:p.Gly90Ala
ENST00000495834.1:c.269G>C	ENSP00000475829.1:p.Gly90Ala
ENST00000535434.5:c.269G>C	ENSP00000443599.1:p.Gly90Ala
ENST00000613953.4:c.626G>C	ENSP00000484435.1:p.Gly209Ala
NM_000365.5:c.515G>C	NP_000356.1:p.Gly172Ala
NM_001159287.1:c.626G>C	NP_001152759.1:p.Gly209Ala
NM_001258026.1:c.269G>C	NP_001244955.1:p.Gly90Ala
XR_002957378.1:n.1248G>C
NM_000365.6:c.515G>C MANE Select	NP_000356.1:p.Gly172Ala
NM_001258026.2:c.269G>C	NP_001244955.1:p.Gly90Ala