Canonical Allele Identifier: CA360969097

Gene: AFF4

Linked Data

• gnomAD v4: 5-132886319-C-G
• MyVariant Identifiers: chr5:g.132222011C>G (hg19) ; chr5:g.132886319C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886319C>G , CM000667.2:g.132886319C>G	GRCh38
NC_000005.9:g.132222011C>G , CM000667.1:g.132222011C>G	GRCh37
NC_000005.8:g.132249910C>G	NCBI36
NG_030340.1:g.82344G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.3090G>C MANE Select	ENSP00000265343.5:p.Glu1030Asp
ENST00000265343.9:c.3090G>C	ENSP00000265343.5:p.Glu1030Asp
NM_014423.3:c.3090G>C	NP_055238.1:p.Glu1030Asp
XM_005271963.3:c.3090G>C	XP_005272020.1:p.Glu1030Asp
XM_005271964.3:c.1956G>C	XP_005272021.1:p.Glu652Asp
XM_006714587.2:c.3003G>C	XP_006714650.1:p.Glu1001Asp
XM_005271963.5:c.3090G>C	XP_005272020.1:p.Glu1030Asp
XM_005271964.4:c.1956G>C	XP_005272021.1:p.Glu652Asp
XM_006714587.4:c.3003G>C	XP_006714650.1:p.Glu1001Asp
NM_014423.4:c.3090G>C MANE Select	NP_055238.1:p.Glu1030Asp