Canonical Allele Identifier: CA446499375

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132269986C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934294C>G , CM000667.2:g.132934294C>G	GRCh38
NC_000005.9:g.132269986C>G , CM000667.1:g.132269986C>G	GRCh37
NC_000005.8:g.132297885C>G	NCBI36
NG_030340.1:g.34369G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.771G>C MANE Select	ENSP00000265343.5:p.Val257=
ENST00000265343.9:c.771G>C	ENSP00000265343.5:p.Val257=
ENST00000378595.7:c.771G>C	ENSP00000367858.3:p.Val257=
ENST00000465484.1:n.1030G>C
ENST00000491831.5:n.1031G>C
NM_014423.3:c.771G>C	NP_055238.1:p.Val257=
XM_005271963.3:c.771G>C	XP_005272020.1:p.Val257=
XM_006714587.2:c.771G>C	XP_006714650.1:p.Val257=
XM_005271963.5:c.771G>C	XP_005272020.1:p.Val257=
XM_006714587.4:c.771G>C	XP_006714650.1:p.Val257=
NM_014423.4:c.771G>C MANE Select	NP_055238.1:p.Val257=