Canonical Allele Identifier: CA446499109

Gene: AFF4

Linked Data

• dbSNP Id: rs1761365494
• gnomAD v4: 5-132934198-G-A
• MyVariant Identifiers: chr5:g.132269890G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934198G>A , CM000667.2:g.132934198G>A	GRCh38
NC_000005.9:g.132269890G>A , CM000667.1:g.132269890G>A	GRCh37
NC_000005.8:g.132297789G>A	NCBI36
NG_030340.1:g.34465C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.867C>T MANE Select	ENSP00000265343.5:p.Pro289=
ENST00000265343.9:c.867C>T	ENSP00000265343.5:p.Pro289=
ENST00000378593.6:n.34C>T
ENST00000378595.7:c.867C>T	ENSP00000367858.3:p.Pro289=
ENST00000425658.1:c.41C>T
ENST00000465484.1:n.1126C>T
ENST00000491831.5:n.1127C>T
NM_014423.3:c.867C>T	NP_055238.1:p.Pro289=
XM_005271963.3:c.867C>T	XP_005272020.1:p.Pro289=
XM_006714587.2:c.867C>T	XP_006714650.1:p.Pro289=
XM_005271963.5:c.867C>T	XP_005272020.1:p.Pro289=
XM_006714587.4:c.867C>T	XP_006714650.1:p.Pro289=
NM_014423.4:c.867C>T MANE Select	NP_055238.1:p.Pro289=