Canonical Allele Identifier: CA691293403

Gene: TPI1

Linked Data

• dbSNP Id: rs1232421394
• gnomAD v3: 12-6870174-T-C
• gnomAD v4: 12-6870174-T-C
• MyVariant Identifiers: chr12:g.6870174T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870174T>C , CM000674.2:g.6870174T>C	GRCh38
NC_000012.11:g.6979338T>C , CM000674.1:g.6979338T>C	GRCh37
NC_000012.10:g.6849599T>C	NCBI36
NG_011948.1:g.7755T>C
NG_013308.1:g.8184A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.631+38T>C MANE Select	ENSP00000379933.4:n.631+38T>C
ENST00000229270.8:c.742+38T>C	ENSP00000229270.4:n.742+38T>C
ENST00000396705.9:c.631+38T>C	ENSP00000379933.4:n.631+38T>C
ENST00000474253.1:n.120+38T>C
ENST00000488464.6:c.385+38T>C	ENSP00000475620.1:n.385+38T>C
ENST00000535434.5:c.385+38T>C	ENSP00000443599.1:n.385+38T>C
ENST00000613953.4:c.742+38T>C	ENSP00000484435.1:n.742+38T>C
NM_000365.5:c.631+38T>C	NP_000356.1:n.631+38T>C
NM_001159287.1:c.742+38T>C	NP_001152759.1:n.742+38T>C
NM_001258026.1:c.385+38T>C	NP_001244955.1:n.385+38T>C
XR_002957378.1:n.1639+38T>C
NM_000365.6:c.631+38T>C MANE Select	NP_000356.1:n.631+38T>C
NM_001258026.2:c.385+38T>C	NP_001244955.1:n.385+38T>C