Canonical Allele Identifier: CA2486362
Gene: TAFA4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.68733148C>T , CM000665.2:g.68733148C>T GRCh38
NC_000003.11:g.68782299C>T , CM000665.1:g.68782299C>T GRCh37
NC_000003.10:g.68864989C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295569.12:c.417G>A MANE Select ENSP00000295569.7:p.Thr139=
ENST00000295569.11:c.417G>A ENSP00000295569.7:p.Thr139=
NM_001005527.2:c.417G>A NP_001005527.1:p.Thr139=
NM_182522.4:c.417G>A NP_872328.1:p.Thr139=
XM_011533371.1:c.376G>A XP_011531673.1:p.Ala126Thr
XM_011533372.1:c.376G>A XP_011531674.1:p.Ala126Thr
NM_182522.5:c.417G>A MANE Select NP_872328.1:p.Thr139=
NM_001005527.3:c.417G>A NP_001005527.1:p.Thr139=