Canonical Allele Identifier: CA446498773
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132228033A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892341A>T , CM000667.2:g.132892341A>T GRCh38
NC_000005.9:g.132228033A>T , CM000667.1:g.132228033A>T GRCh37
NC_000005.8:g.132255932A>T NCBI36
NG_030340.1:g.76322T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2460T>A MANE Select ENSP00000265343.5:p.Pro820=
ENST00000265343.9:c.2460T>A ENSP00000265343.5:p.Pro820=
ENST00000378595.7:c.2460T>A ENSP00000367858.3:p.Pro820=
NM_014423.3:c.2460T>A NP_055238.1:p.Pro820=
XM_005271963.3:c.2460T>A XP_005272020.1:p.Pro820=
XM_005271964.3:c.1326T>A XP_005272021.1:p.Pro442=
XM_006714587.2:c.2373T>A XP_006714650.1:p.Pro791=
XM_005271963.5:c.2460T>A XP_005272020.1:p.Pro820=
XM_005271964.4:c.1326T>A XP_005272021.1:p.Pro442=
XM_006714587.4:c.2373T>A XP_006714650.1:p.Pro791=
NM_014423.4:c.2460T>A MANE Select NP_055238.1:p.Pro820=