Canonical Allele Identifier: CA127299651
Community Standard Title: NM_014423.4(AFF4):c.3365-189G>T
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132881375C>A , CM000667.2:g.132881375C>A GRCh38
NC_000005.9:g.132217067C>A , CM000667.1:g.132217067C>A GRCh37
NC_000005.8:g.132244966C>A NCBI36
NG_030340.1:g.87288G>T

Transcript Alleles

HGVS Amino-acid Change
NM_014423.4:c.3365-189G>T MANE Select NP_055238.1:n.3365-189G>T
ENST00000265343.10:c.3365-189G>T MANE Select ENSP00000265343.5:n.3365-189G>T
NM_014423.3:c.3365-189G>T NP_055238.1:n.3365-189G>T
ENST00000265343.9:c.3365-189G>T ENSP00000265343.5:n.3365-189G>T
XM_005271963.3:c.3365-189G>T XP_005272020.1:n.3365-189G>T
XM_005271963.5:c.3365-189G>T XP_005272020.1:n.3365-189G>T
XM_005271964.3:c.2231-189G>T XP_005272021.1:n.2231-189G>T
XM_005271964.4:c.2231-189G>T XP_005272021.1:n.2231-189G>T
XM_006714587.2:c.3278-189G>T XP_006714650.1:n.3278-189G>T
XM_006714587.4:c.3278-189G>T XP_006714650.1:n.3278-189G>T