Canonical Allele Identifier: CA446377145

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132222014T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886322T>C , CM000667.2:g.132886322T>C	GRCh38
NC_000005.9:g.132222014T>C , CM000667.1:g.132222014T>C	GRCh37
NC_000005.8:g.132249913T>C	NCBI36
NG_030340.1:g.82341A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.3087A>G MANE Select	ENSP00000265343.5:p.Thr1029=
ENST00000265343.9:c.3087A>G	ENSP00000265343.5:p.Thr1029=
NM_014423.3:c.3087A>G	NP_055238.1:p.Thr1029=
XM_005271963.3:c.3087A>G	XP_005272020.1:p.Thr1029=
XM_005271964.3:c.1953A>G	XP_005272021.1:p.Thr651=
XM_006714587.2:c.3000A>G	XP_006714650.1:p.Thr1000=
XM_005271963.5:c.3087A>G	XP_005272020.1:p.Thr1029=
XM_005271964.4:c.1953A>G	XP_005272021.1:p.Thr651=
XM_006714587.4:c.3000A>G	XP_006714650.1:p.Thr1000=
NM_014423.4:c.3087A>G MANE Select	NP_055238.1:p.Thr1029=