Canonical Allele Identifier: CA1522097464
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437813G= , CM000667.2:g.437813G= GRCh38
NC_000005.9:g.437928G= , CM000667.1:g.437928G= GRCh37
NC_000005.8:g.490928G= NCBI36
NG_029834.1:g.138638G=
NG_029834.2:g.138638G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*2979G= (AHRR) MANE Select ENSP00000507476.1:n.*2979G=
ENST00000316418.10:c.*2979G= (AHRR) ENSP00000323816.6:n.*2979G=
ENST00000505113.6:c.*5069G= (PDCD6-AHRR) ENSP00000424601.2:n.*5069G=
ENST00000675395.1:c.*5123G= (PDCD6-AHRR) ENSP00000502570.1:n.*5123G=
ENST00000316418.9:c.*2979G= (AHRR) ENSP00000323816.5:n.*2979G=
NM_001242412.1:c.*2979G= (AHRR) NP_001229341.1:n.*2979G=
NM_020731.4:c.*2979G= (AHRR) NP_065782.2:n.*2979G=
NM_001377236.1:c.*2979G= (AHRR) MANE Select NP_001364165.1:n.*2979G=
NM_001377239.1:c.*2979G= (AHRR) NP_001364168.1:n.*2979G=
NR_165159.2:n.5420G= (PDCD6-AHRR)
NR_165163.2:n.5366G= (PDCD6-AHRR)