Canonical Allele Identifier: CA446498904
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132228003A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892311A>T , CM000667.2:g.132892311A>T GRCh38
NC_000005.9:g.132228003A>T , CM000667.1:g.132228003A>T GRCh37
NC_000005.8:g.132255902A>T NCBI36
NG_030340.1:g.76352T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.2490T>A MANE Select ENSP00000265343.5:p.Ser830=
ENST00000265343.9:c.2490T>A ENSP00000265343.5:p.Ser830=
ENST00000378595.7:c.2490T>A ENSP00000367858.3:p.Ser830=
NM_014423.3:c.2490T>A NP_055238.1:p.Ser830=
XM_005271963.3:c.2490T>A XP_005272020.1:p.Ser830=
XM_005271964.3:c.1356T>A XP_005272021.1:p.Ser452=
XM_006714587.2:c.2403T>A XP_006714650.1:p.Ser801=
XM_005271963.5:c.2490T>A XP_005272020.1:p.Ser830=
XM_005271964.4:c.1356T>A XP_005272021.1:p.Ser452=
XM_006714587.4:c.2403T>A XP_006714650.1:p.Ser801=
NM_014423.4:c.2490T>A MANE Select NP_055238.1:p.Ser830=