Canonical Allele Identifier: CA446499418

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132269998G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132934306G>C , CM000667.2:g.132934306G>C	GRCh38
NC_000005.9:g.132269998G>C , CM000667.1:g.132269998G>C	GRCh37
NC_000005.8:g.132297897G>C	NCBI36
NG_030340.1:g.34357C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.759C>G MANE Select	ENSP00000265343.5:p.Pro253=
ENST00000265343.9:c.759C>G	ENSP00000265343.5:p.Pro253=
ENST00000378595.7:c.759C>G	ENSP00000367858.3:p.Pro253=
ENST00000465484.1:n.1018C>G
ENST00000491831.5:n.1019C>G
NM_014423.3:c.759C>G	NP_055238.1:p.Pro253=
XM_005271963.3:c.759C>G	XP_005272020.1:p.Pro253=
XM_006714587.2:c.759C>G	XP_006714650.1:p.Pro253=
XM_005271963.5:c.759C>G	XP_005272020.1:p.Pro253=
XM_006714587.4:c.759C>G	XP_006714650.1:p.Pro253=
NM_014423.4:c.759C>G MANE Select	NP_055238.1:p.Pro253=