Canonical Allele Identifier: CA1522097454

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs1737156459

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437795G>C , CM000667.2:g.437795G>C	GRCh38
NC_000005.9:g.437910G>C , CM000667.1:g.437910G>C	GRCh37
NC_000005.8:g.490910G>C	NCBI36
NG_029834.1:g.138620G>C
NG_029834.2:g.138620G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684583.1:c.*2961G>C (AHRR) MANE Select	ENSP00000507476.1:n.*2961G>C
ENST00000316418.10:c.*2961G>C (AHRR)	ENSP00000323816.6:n.*2961G>C
ENST00000505113.6:c.*5051G>C (PDCD6-AHRR)	ENSP00000424601.2:n.*5051G>C
ENST00000675395.1:c.*5105G>C (PDCD6-AHRR)	ENSP00000502570.1:n.*5105G>C
ENST00000316418.9:c.*2961G>C (AHRR)	ENSP00000323816.5:n.*2961G>C
NM_001242412.1:c.*2961G>C (AHRR)	NP_001229341.1:n.*2961G>C
NM_020731.4:c.*2961G>C (AHRR)	NP_065782.2:n.*2961G>C
NM_001377236.1:c.*2961G>C (AHRR) MANE Select	NP_001364165.1:n.*2961G>C
NM_001377239.1:c.*2961G>C (AHRR)	NP_001364168.1:n.*2961G>C
NR_165159.2:n.5402G>C (PDCD6-AHRR)
NR_165163.2:n.5348G>C (PDCD6-AHRR)