Canonical Allele Identifier: CA804039632

Gene: AFF4

Linked Data

• dbSNP Id: rs1294096966
• gnomAD v3: 5-132886210-TG-T
• gnomAD v4: 5-132886210-TG-T
• MyVariant Identifiers: chr5:g.132221903del (hg19) ; chr5:g.132886211del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886212del , CM000667.2:g.132886212del	GRCh38
NC_000005.9:g.132221904del , CM000667.1:g.132221904del	GRCh37
NC_000005.8:g.132249803del	NCBI36
NG_030340.1:g.82452del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.3099+99del MANE Select	ENSP00000265343.5:n.3099+99del
ENST00000265343.9:c.3099+99del	ENSP00000265343.5:n.3099+99del
NM_014423.3:c.3099+99del	NP_055238.1:n.3099+99del
XM_005271963.3:c.3099+99del	XP_005272020.1:n.3099+99del
XM_005271964.3:c.1965+99del	XP_005272021.1:n.1965+99del
XM_006714587.2:c.3012+99del	XP_006714650.1:n.3012+99del
XM_005271963.5:c.3099+99del	XP_005272020.1:n.3099+99del
XM_005271964.4:c.1965+99del	XP_005272021.1:n.1965+99del
XM_006714587.4:c.3012+99del	XP_006714650.1:n.3012+99del
NM_014423.4:c.3099+99del MANE Select	NP_055238.1:n.3099+99del