Canonical Allele Identifier: CA478163787
Gene: TPI1 HGNC NCBI

Linked Data

dbSNP Id: rs1442155961
gnomAD v2: 12-6976691-G-T
gnomAD v3: 12-6867527-G-T
gnomAD v4: 12-6867527-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6867527G>T , CM000674.2:g.6867527G>T GRCh38
NC_000012.11:g.6976691G>T , CM000674.1:g.6976691G>T GRCh37
NC_000012.10:g.6846952G>T NCBI36
NG_011948.1:g.5108G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229270.8:c.72G>T ENSP00000229270.4:p.Leu24=
ENST00000613953.4:c.72G>T ENSP00000484435.1:p.Leu24=
NM_001159287.1:c.72G>T NP_001152759.1:p.Leu24=
XR_002957378.1:n.694G>T