Canonical Allele Identifier: CA127270695
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132893064T>G , CM000667.2:g.132893064T>G GRCh38
NC_000005.9:g.132228756T>G , CM000667.1:g.132228756T>G GRCh37
NC_000005.8:g.132256655T>G NCBI36
NG_030340.1:g.75599A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2362A>C MANE Select ENSP00000265343.5:p.Asn788His
ENST00000265343.9:c.2362A>C ENSP00000265343.5:p.Asn788His
ENST00000378595.7:c.2362A>C ENSP00000367858.3:p.Asn788His
NM_014423.3:c.2362A>C NP_055238.1:p.Asn788His
XM_005271963.3:c.2362A>C XP_005272020.1:p.Asn788His
XM_005271964.3:c.1228A>C XP_005272021.1:p.Asn410His
XM_006714587.2:c.2275A>C XP_006714650.1:p.Asn759His
XM_005271963.5:c.2362A>C XP_005272020.1:p.Asn788His
XM_005271964.4:c.1228A>C XP_005272021.1:p.Asn410His
XM_006714587.4:c.2275A>C XP_006714650.1:p.Asn759His
NM_014423.4:c.2362A>C MANE Select NP_055238.1:p.Asn788His