Canonical Allele Identifier: CA446373353
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132881140A>G , CM000667.2:g.132881140A>G GRCh38
NC_000005.9:g.132216832A>G , CM000667.1:g.132216832A>G GRCh37
NC_000005.8:g.132244731A>G NCBI36
NG_030340.1:g.87523T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3411T>C MANE Select ENSP00000265343.5:p.Asn1137=
ENST00000265343.9:c.3411T>C ENSP00000265343.5:p.Asn1137=
NM_014423.3:c.3411T>C NP_055238.1:p.Asn1137=
XM_005271963.3:c.3411T>C XP_005272020.1:p.Asn1137=
XM_005271964.3:c.2277T>C XP_005272021.1:p.Asn759=
XM_006714587.2:c.3324T>C XP_006714650.1:p.Asn1108=
XM_005271963.5:c.3411T>C XP_005272020.1:p.Asn1137=
XM_005271964.4:c.2277T>C XP_005272021.1:p.Asn759=
XM_006714587.4:c.3324T>C XP_006714650.1:p.Asn1108=
NM_014423.4:c.3411T>C MANE Select NP_055238.1:p.Asn1137=