Canonical Allele Identifier: CA446499370
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132269985G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934293G>T , CM000667.2:g.132934293G>T GRCh38
NC_000005.9:g.132269985G>T , CM000667.1:g.132269985G>T GRCh37
NC_000005.8:g.132297884G>T NCBI36
NG_030340.1:g.34370C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.772C>A MANE Select ENSP00000265343.5:p.Arg258=
ENST00000265343.9:c.772C>A ENSP00000265343.5:p.Arg258=
ENST00000378595.7:c.772C>A ENSP00000367858.3:p.Arg258=
ENST00000465484.1:n.1031C>A
ENST00000491831.5:n.1032C>A
NM_014423.3:c.772C>A NP_055238.1:p.Arg258=
XM_005271963.3:c.772C>A XP_005272020.1:p.Arg258=
XM_006714587.2:c.772C>A XP_006714650.1:p.Arg258=
XM_005271963.5:c.772C>A XP_005272020.1:p.Arg258=
XM_006714587.4:c.772C>A XP_006714650.1:p.Arg258=
NM_014423.4:c.772C>A MANE Select NP_055238.1:p.Arg258=