Canonical Allele Identifier: CA446499417
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132269998G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934306G>A , CM000667.2:g.132934306G>A GRCh38
NC_000005.9:g.132269998G>A , CM000667.1:g.132269998G>A GRCh37
NC_000005.8:g.132297897G>A NCBI36
NG_030340.1:g.34357C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.759C>T MANE Select ENSP00000265343.5:p.Pro253=
ENST00000265343.9:c.759C>T ENSP00000265343.5:p.Pro253=
ENST00000378595.7:c.759C>T ENSP00000367858.3:p.Pro253=
ENST00000465484.1:n.1018C>T
ENST00000491831.5:n.1019C>T
NM_014423.3:c.759C>T NP_055238.1:p.Pro253=
XM_005271963.3:c.759C>T XP_005272020.1:p.Pro253=
XM_006714587.2:c.759C>T XP_006714650.1:p.Pro253=
XM_005271963.5:c.759C>T XP_005272020.1:p.Pro253=
XM_006714587.4:c.759C>T XP_006714650.1:p.Pro253=
NM_014423.4:c.759C>T MANE Select NP_055238.1:p.Pro253=