Canonical Allele Identifier: CA446499413
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132269995A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934303A>T , CM000667.2:g.132934303A>T GRCh38
NC_000005.9:g.132269995A>T , CM000667.1:g.132269995A>T GRCh37
NC_000005.8:g.132297894A>T NCBI36
NG_030340.1:g.34360T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.762T>A MANE Select ENSP00000265343.5:p.Thr254=
ENST00000265343.9:c.762T>A ENSP00000265343.5:p.Thr254=
ENST00000378595.7:c.762T>A ENSP00000367858.3:p.Thr254=
ENST00000465484.1:n.1021T>A
ENST00000491831.5:n.1022T>A
NM_014423.3:c.762T>A NP_055238.1:p.Thr254=
XM_005271963.3:c.762T>A XP_005272020.1:p.Thr254=
XM_006714587.2:c.762T>A XP_006714650.1:p.Thr254=
XM_005271963.5:c.762T>A XP_005272020.1:p.Thr254=
XM_006714587.4:c.762T>A XP_006714650.1:p.Thr254=
NM_014423.4:c.762T>A MANE Select NP_055238.1:p.Thr254=