Canonical Allele Identifier: CA446499115
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132269893C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934201C>T , CM000667.2:g.132934201C>T GRCh38
NC_000005.9:g.132269893C>T , CM000667.1:g.132269893C>T GRCh37
NC_000005.8:g.132297792C>T NCBI36
NG_030340.1:g.34462G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.864G>A MANE Select ENSP00000265343.5:p.Lys288=
ENST00000265343.9:c.864G>A ENSP00000265343.5:p.Lys288=
ENST00000378593.6:n.31G>A
ENST00000378595.7:c.864G>A ENSP00000367858.3:p.Lys288=
ENST00000425658.1:c.38G>A
ENST00000465484.1:n.1123G>A
ENST00000491831.5:n.1124G>A
NM_014423.3:c.864G>A NP_055238.1:p.Lys288=
XM_005271963.3:c.864G>A XP_005272020.1:p.Lys288=
XM_006714587.2:c.864G>A XP_006714650.1:p.Lys288=
XM_005271963.5:c.864G>A XP_005272020.1:p.Lys288=
XM_006714587.4:c.864G>A XP_006714650.1:p.Lys288=
NM_014423.4:c.864G>A MANE Select NP_055238.1:p.Lys288=