Canonical Allele Identifier: CA360958256

Gene: AFF4

Linked Data

• ClinVar Variation Id: 2121344
• ClinVar RCV Id: RCV003049112
• MyVariant Identifiers: chr5:g.132269993G>A (hg19) ; chr5:g.132934301G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934301G>A , CM000667.2:g.132934301G>A	GRCh38
NC_000005.9:g.132269993G>A , CM000667.1:g.132269993G>A	GRCh37
NC_000005.8:g.132297892G>A	NCBI36
NG_030340.1:g.34362C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.764C>T MANE Select	ENSP00000265343.5:p.Ala255Val
ENST00000265343.9:c.764C>T	ENSP00000265343.5:p.Ala255Val
ENST00000378595.7:c.764C>T	ENSP00000367858.3:p.Ala255Val
ENST00000465484.1:n.1023C>T
ENST00000491831.5:n.1024C>T
NM_014423.3:c.764C>T	NP_055238.1:p.Ala255Val
XM_005271963.3:c.764C>T	XP_005272020.1:p.Ala255Val
XM_006714587.2:c.764C>T	XP_006714650.1:p.Ala255Val
XM_005271963.5:c.764C>T	XP_005272020.1:p.Ala255Val
XM_006714587.4:c.764C>T	XP_006714650.1:p.Ala255Val
NM_014423.4:c.764C>T MANE Select	NP_055238.1:p.Ala255Val