Canonical Allele Identifier: CA1522097564
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

dbSNP Id: rs1737169111

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.438033A>G , CM000667.2:g.438033A>G GRCh38
NC_000005.9:g.438148A>G , CM000667.1:g.438148A>G GRCh37
NC_000005.8:g.491148A>G NCBI36
NG_029834.1:g.138858A>G
NG_029834.2:g.138858A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3199A>G (AHRR) MANE Select ENSP00000507476.1:n.*3199A>G
ENST00000316418.10:c.*3199A>G (AHRR) ENSP00000323816.6:n.*3199A>G
ENST00000505113.6:c.*5289A>G (PDCD6-AHRR) ENSP00000424601.2:n.*5289A>G
ENST00000675395.1:c.*5343A>G (PDCD6-AHRR) ENSP00000502570.1:n.*5343A>G
ENST00000316418.9:c.*3199A>G (AHRR) ENSP00000323816.5:n.*3199A>G
NM_001242412.1:c.*3199A>G (AHRR) NP_001229341.1:n.*3199A>G
NM_020731.4:c.*3199A>G (AHRR) NP_065782.2:n.*3199A>G
NM_001377236.1:c.*3199A>G (AHRR) MANE Select NP_001364165.1:n.*3199A>G
NM_001377239.1:c.*3199A>G (AHRR) NP_001364168.1:n.*3199A>G
NR_165159.2:n.5640A>G (PDCD6-AHRR)
NR_165163.2:n.5586A>G (PDCD6-AHRR)