Canonical Allele Identifier: CA446498850

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132227910T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892218T>C , CM000667.2:g.132892218T>C	GRCh38
NC_000005.9:g.132227910T>C , CM000667.1:g.132227910T>C	GRCh37
NC_000005.8:g.132255809T>C	NCBI36
NG_030340.1:g.76445A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.2583A>G MANE Select	ENSP00000265343.5:p.Thr861=
ENST00000265343.9:c.2583A>G	ENSP00000265343.5:p.Thr861=
ENST00000378595.7:c.2583A>G	ENSP00000367858.3:p.Thr861=
NM_014423.3:c.2583A>G	NP_055238.1:p.Thr861=
XM_005271963.3:c.2583A>G	XP_005272020.1:p.Thr861=
XM_005271964.3:c.1449A>G	XP_005272021.1:p.Thr483=
XM_006714587.2:c.2496A>G	XP_006714650.1:p.Thr832=
XM_005271963.5:c.2583A>G	XP_005272020.1:p.Thr861=
XM_005271964.4:c.1449A>G	XP_005272021.1:p.Thr483=
XM_006714587.4:c.2496A>G	XP_006714650.1:p.Thr832=
NM_014423.4:c.2583A>G MANE Select	NP_055238.1:p.Thr861=