Canonical Allele Identifier: CA446499110

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132269890G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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