Canonical Allele Identifier: CA446499128

Gene: AFF4

Linked Data

• gnomAD v4: 5-132934204-C-A
• MyVariant Identifiers: chr5:g.132269896C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934204C>A , CM000667.2:g.132934204C>A	GRCh38
NC_000005.9:g.132269896C>A , CM000667.1:g.132269896C>A	GRCh37
NC_000005.8:g.132297795C>A	NCBI36
NG_030340.1:g.34459G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.861G>T MANE Select	ENSP00000265343.5:p.Leu287=
ENST00000265343.9:c.861G>T	ENSP00000265343.5:p.Leu287=
ENST00000378593.6:n.28G>T
ENST00000378595.7:c.861G>T	ENSP00000367858.3:p.Leu287=
ENST00000425658.1:c.35G>T
ENST00000465484.1:n.1120G>T
ENST00000491831.5:n.1121G>T
NM_014423.3:c.861G>T	NP_055238.1:p.Leu287=
XM_005271963.3:c.861G>T	XP_005272020.1:p.Leu287=
XM_006714587.2:c.861G>T	XP_006714650.1:p.Leu287=
XM_005271963.5:c.861G>T	XP_005272020.1:p.Leu287=
XM_006714587.4:c.861G>T	XP_006714650.1:p.Leu287=
NM_014423.4:c.861G>T MANE Select	NP_055238.1:p.Leu287=