Canonical Allele Identifier: CA2617355462

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870385-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870385C>G , CM000674.2:g.6870385C>G	GRCh38
NC_000012.11:g.6979549C>G , CM000674.1:g.6979549C>G	GRCh37
NC_000012.10:g.6849810C>G	NCBI36
NG_011948.1:g.7966C>G
NG_013308.1:g.7973G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*2C>G MANE Select	ENSP00000379933.4:n.*2C>G
ENST00000229270.8:c.*2C>G	ENSP00000229270.4:n.*2C>G
ENST00000396705.9:c.*2C>G	ENSP00000379933.4:n.*2C>G
ENST00000474253.1:n.241C>G
ENST00000535434.5:c.*2C>G	ENSP00000443599.1:n.*2C>G
ENST00000613953.4:c.*2C>G	ENSP00000484435.1:n.*2C>G
NM_000365.5:c.*2C>G	NP_000356.1:n.*2C>G
NM_001159287.1:c.*2C>G	NP_001152759.1:n.*2C>G
NM_001258026.1:c.*2C>G	NP_001244955.1:n.*2C>G
XR_002957378.1:n.1760C>G
NM_000365.6:c.*2C>G MANE Select	NP_000356.1:n.*2C>G
NM_001258026.2:c.*2C>G	NP_001244955.1:n.*2C>G