Canonical Allele Identifier: CA360969442
Gene: AFF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886396A>G , CM000667.2:g.132886396A>G GRCh38
NC_000005.9:g.132222088A>G , CM000667.1:g.132222088A>G GRCh37
NC_000005.8:g.132249987A>G NCBI36
NG_030340.1:g.82267T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3013T>C MANE Select ENSP00000265343.5:p.Cys1005Arg
ENST00000265343.9:c.3013T>C ENSP00000265343.5:p.Cys1005Arg
NM_014423.3:c.3013T>C NP_055238.1:p.Cys1005Arg
XM_005271963.3:c.3013T>C XP_005272020.1:p.Cys1005Arg
XM_005271964.3:c.1879T>C XP_005272021.1:p.Cys627Arg
XM_006714587.2:c.2926T>C XP_006714650.1:p.Cys976Arg
XM_005271963.5:c.3013T>C XP_005272020.1:p.Cys1005Arg
XM_005271964.4:c.1879T>C XP_005272021.1:p.Cys627Arg
XM_006714587.4:c.2926T>C XP_006714650.1:p.Cys976Arg
NM_014423.4:c.3013T>C MANE Select NP_055238.1:p.Cys1005Arg