Canonical Allele Identifier: CA1522097559
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.438019T= , CM000667.2:g.438019T= GRCh38
NC_000005.9:g.438134T= , CM000667.1:g.438134T= GRCh37
NC_000005.8:g.491134T= NCBI36
NG_029834.1:g.138844T=
NG_029834.2:g.138844T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3185T= (AHRR) MANE Select ENSP00000507476.1:n.*3185T=
ENST00000316418.10:c.*3185T= (AHRR) ENSP00000323816.6:n.*3185T=
ENST00000505113.6:c.*5275T= (PDCD6-AHRR) ENSP00000424601.2:n.*5275T=
ENST00000675395.1:c.*5329T= (PDCD6-AHRR) ENSP00000502570.1:n.*5329T=
ENST00000316418.9:c.*3185T= (AHRR) ENSP00000323816.5:n.*3185T=
NM_001242412.1:c.*3185T= (AHRR) NP_001229341.1:n.*3185T=
NM_020731.4:c.*3185T= (AHRR) NP_065782.2:n.*3185T=
NM_001377236.1:c.*3185T= (AHRR) MANE Select NP_001364165.1:n.*3185T=
NM_001377239.1:c.*3185T= (AHRR) NP_001364168.1:n.*3185T=
NR_165159.2:n.5626T= (PDCD6-AHRR)
NR_165163.2:n.5572T= (PDCD6-AHRR)