Canonical Allele Identifier: CA199677

Gene: AFF4

Linked Data

• ClinVar Variation Id: 190329
• ClinVar RCV Id: RCV000170515
• dbSNP Id: rs786205233
• MyVariant Identifiers: chr5:g.132269997T>C (hg19) ; chr5:g.132934305T>C (hg38)
• PubMed: PMID:25730767

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934305T>C , CM000667.2:g.132934305T>C	GRCh38
NC_000005.9:g.132269997T>C , CM000667.1:g.132269997T>C	GRCh37
NC_000005.8:g.132297896T>C	NCBI36
NG_030340.1:g.34358A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.760A>G MANE Select	ENSP00000265343.5:p.Thr254Ala
ENST00000265343.9:c.760A>G	ENSP00000265343.5:p.Thr254Ala
ENST00000378595.7:c.760A>G	ENSP00000367858.3:p.Thr254Ala
ENST00000465484.1:n.1019A>G
ENST00000491831.5:n.1020A>G
NM_014423.3:c.760A>G	NP_055238.1:p.Thr254Ala
XM_005271963.3:c.760A>G	XP_005272020.1:p.Thr254Ala
XM_006714587.2:c.760A>G	XP_006714650.1:p.Thr254Ala
XM_005271963.5:c.760A>G	XP_005272020.1:p.Thr254Ala
XM_006714587.4:c.760A>G	XP_006714650.1:p.Thr254Ala
NM_014423.4:c.760A>G MANE Select	NP_055238.1:p.Thr254Ala