Canonical Allele Identifier: CA1522097484
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437860G= , CM000667.2:g.437860G= GRCh38
NC_000005.9:g.437975G= , CM000667.1:g.437975G= GRCh37
NC_000005.8:g.490975G= NCBI36
NG_029834.1:g.138685G=
NG_029834.2:g.138685G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3026G= (AHRR) MANE Select ENSP00000507476.1:n.*3026G=
ENST00000316418.10:c.*3026G= (AHRR) ENSP00000323816.6:n.*3026G=
ENST00000505113.6:c.*5116G= (PDCD6-AHRR) ENSP00000424601.2:n.*5116G=
ENST00000675395.1:c.*5170G= (PDCD6-AHRR) ENSP00000502570.1:n.*5170G=
ENST00000316418.9:c.*3026G= (AHRR) ENSP00000323816.5:n.*3026G=
NM_001242412.1:c.*3026G= (AHRR) NP_001229341.1:n.*3026G=
NM_020731.4:c.*3026G= (AHRR) NP_065782.2:n.*3026G=
NM_001377236.1:c.*3026G= (AHRR) MANE Select NP_001364165.1:n.*3026G=
NM_001377239.1:c.*3026G= (AHRR) NP_001364168.1:n.*3026G=
NR_165159.2:n.5467G= (PDCD6-AHRR)
NR_165163.2:n.5413G= (PDCD6-AHRR)