Canonical Allele Identifier: CA1522097546
Community Standard Title: NM_001377236.1(AHRR):c.*3153G=
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437987G= , CM000667.2:g.437987G= GRCh38
NC_000005.9:g.438102G= , CM000667.1:g.438102G= GRCh37
NC_000005.8:g.491102G= NCBI36
NG_029834.1:g.138812G=
NG_029834.2:g.138812G=

Transcript Alleles

HGVS Amino-acid Change
NM_001377236.1:c.*3153G= (AHRR) MANE Select NP_001364165.1:n.*3153G=
ENST00000684583.1:c.*3153G= (AHRR) MANE Select ENSP00000507476.1:n.*3153G=
NM_001242412.1:c.*3153G= (AHRR) NP_001229341.1:n.*3153G=
NM_001377239.1:c.*3153G= (AHRR) NP_001364168.1:n.*3153G=
NM_020731.4:c.*3153G= (AHRR) NP_065782.2:n.*3153G=
NR_165159.2:n.5594G= (PDCD6-AHRR)
NR_165163.2:n.5540G= (PDCD6-AHRR)
ENST00000316418.10:c.*3153G= (AHRR) ENSP00000323816.6:n.*3153G=
ENST00000316418.9:c.*3153G= (AHRR) ENSP00000323816.5:n.*3153G=
ENST00000505113.6:c.*5243G= (PDCD6-AHRR) ENSP00000424601.2:n.*5243G=
ENST00000675395.1:c.*5297G= (PDCD6-AHRR) ENSP00000502570.1:n.*5297G=