Canonical Allele Identifier: CA446377335

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132222065C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886373C>T , CM000667.2:g.132886373C>T	GRCh38
NC_000005.9:g.132222065C>T , CM000667.1:g.132222065C>T	GRCh37
NC_000005.8:g.132249964C>T	NCBI36
NG_030340.1:g.82290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.3036G>A MANE Select	ENSP00000265343.5:p.Arg1012=
ENST00000265343.9:c.3036G>A	ENSP00000265343.5:p.Arg1012=
NM_014423.3:c.3036G>A	NP_055238.1:p.Arg1012=
XM_005271963.3:c.3036G>A	XP_005272020.1:p.Arg1012=
XM_005271964.3:c.1902G>A	XP_005272021.1:p.Arg634=
XM_006714587.2:c.2949G>A	XP_006714650.1:p.Arg983=
XM_005271963.5:c.3036G>A	XP_005272020.1:p.Arg1012=
XM_005271964.4:c.1902G>A	XP_005272021.1:p.Arg634=
XM_006714587.4:c.2949G>A	XP_006714650.1:p.Arg983=
NM_014423.4:c.3036G>A MANE Select	NP_055238.1:p.Arg1012=