Canonical Allele Identifier: CA446377353
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132222070G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886378G>A , CM000667.2:g.132886378G>A GRCh38
NC_000005.9:g.132222070G>A , CM000667.1:g.132222070G>A GRCh37
NC_000005.8:g.132249969G>A NCBI36
NG_030340.1:g.82285C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3031C>T MANE Select ENSP00000265343.5:p.Leu1011=
ENST00000265343.9:c.3031C>T ENSP00000265343.5:p.Leu1011=
NM_014423.3:c.3031C>T NP_055238.1:p.Leu1011=
XM_005271963.3:c.3031C>T XP_005272020.1:p.Leu1011=
XM_005271964.3:c.1897C>T XP_005272021.1:p.Leu633=
XM_006714587.2:c.2944C>T XP_006714650.1:p.Leu982=
XM_005271963.5:c.3031C>T XP_005272020.1:p.Leu1011=
XM_005271964.4:c.1897C>T XP_005272021.1:p.Leu633=
XM_006714587.4:c.2944C>T XP_006714650.1:p.Leu982=
NM_014423.4:c.3031C>T MANE Select NP_055238.1:p.Leu1011=