Canonical Allele Identifier: CA446377141

Gene: AFF4

Linked Data

• MyVariant Identifiers: chr5:g.132222005C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886313C>G , CM000667.2:g.132886313C>G	GRCh38
NC_000005.9:g.132222005C>G , CM000667.1:g.132222005C>G	GRCh37
NC_000005.8:g.132249904C>G	NCBI36
NG_030340.1:g.82350G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.3096G>C MANE Select	ENSP00000265343.5:p.Leu1032=
ENST00000265343.9:c.3096G>C	ENSP00000265343.5:p.Leu1032=
NM_014423.3:c.3096G>C	NP_055238.1:p.Leu1032=
XM_005271963.3:c.3096G>C	XP_005272020.1:p.Leu1032=
XM_005271964.3:c.1962G>C	XP_005272021.1:p.Leu654=
XM_006714587.2:c.3009G>C	XP_006714650.1:p.Leu1003=
XM_005271963.5:c.3096G>C	XP_005272020.1:p.Leu1032=
XM_005271964.4:c.1962G>C	XP_005272021.1:p.Leu654=
XM_006714587.4:c.3009G>C	XP_006714650.1:p.Leu1003=
NM_014423.4:c.3096G>C MANE Select	NP_055238.1:p.Leu1032=