Canonical Allele Identifier: CA3408780
Community Standard Title: NM_014423.4(AFF4):c.2995A>G (p.Thr999Ala)
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132887531T>C , CM000667.2:g.132887531T>C GRCh38
NC_000005.9:g.132223223T>C , CM000667.1:g.132223223T>C GRCh37
NC_000005.8:g.132251122T>C NCBI36
NG_030340.1:g.81132A>G

Transcript Alleles

HGVS Amino-acid Change
NM_014423.4:c.2995A>G MANE Select NP_055238.1:p.Thr999Ala
ENST00000265343.10:c.2995A>G MANE Select ENSP00000265343.5:p.Thr999Ala
NM_014423.3:c.2995A>G NP_055238.1:p.Thr999Ala
ENST00000265343.9:c.2995A>G ENSP00000265343.5:p.Thr999Ala
XM_005271963.3:c.2995A>G XP_005272020.1:p.Thr999Ala
XM_005271963.5:c.2995A>G XP_005272020.1:p.Thr999Ala
XM_005271964.3:c.1861A>G XP_005272021.1:p.Thr621Ala
XM_005271964.4:c.1861A>G XP_005272021.1:p.Thr621Ala
XM_006714587.2:c.2908A>G XP_006714650.1:p.Thr970Ala
XM_006714587.4:c.2908A>G XP_006714650.1:p.Thr970Ala