Canonical Allele Identifier: CA383712691

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870049-G-C
• MyVariant Identifiers: chr12:g.6979213G>C (hg19) ; chr12:g.6870049G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870049G>C , CM000674.2:g.6870049G>C	GRCh38
NC_000012.11:g.6979213G>C , CM000674.1:g.6979213G>C	GRCh37
NC_000012.10:g.6849474G>C	NCBI36
NG_011948.1:g.7630G>C
NG_013308.1:g.8309C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.544G>C MANE Select	ENSP00000379933.4:p.Ala182Pro
ENST00000229270.8:c.655G>C	ENSP00000229270.4:p.Ala219Pro
ENST00000396705.9:c.544G>C	ENSP00000379933.4:p.Ala182Pro
ENST00000474253.1:n.33G>C
ENST00000482209.1:n.240G>C
ENST00000488464.6:c.298G>C	ENSP00000475620.1:p.Ala100Pro
ENST00000493987.5:c.298G>C	ENSP00000475364.1:p.Ala100Pro
ENST00000535434.5:c.298G>C	ENSP00000443599.1:p.Ala100Pro
ENST00000613953.4:c.655G>C	ENSP00000484435.1:p.Ala219Pro
NM_000365.5:c.544G>C	NP_000356.1:p.Ala182Pro
NM_001159287.1:c.655G>C	NP_001152759.1:p.Ala219Pro
NM_001258026.1:c.298G>C	NP_001244955.1:p.Ala100Pro
XR_002957378.1:n.1552G>C
NM_000365.6:c.544G>C MANE Select	NP_000356.1:p.Ala182Pro
NM_001258026.2:c.298G>C	NP_001244955.1:p.Ala100Pro