Canonical Allele Identifier: CA810916312

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs1424743218
• gnomAD v4: 5-437840-A-G
• MyVariant Identifiers: chr5:g.437955A>G (hg19) ; chr5:g.437840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437840A>G , CM000667.2:g.437840A>G	GRCh38
NC_000005.9:g.437955A>G , CM000667.1:g.437955A>G	GRCh37
NC_000005.8:g.490955A>G	NCBI36
NG_029834.1:g.138665A>G
NG_029834.2:g.138665A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684583.1:c.*3006A>G (AHRR) MANE Select	ENSP00000507476.1:n.*3006A>G
ENST00000316418.10:c.*3006A>G (AHRR)	ENSP00000323816.6:n.*3006A>G
ENST00000505113.6:c.*5096A>G (PDCD6-AHRR)	ENSP00000424601.2:n.*5096A>G
ENST00000675395.1:c.*5150A>G (PDCD6-AHRR)	ENSP00000502570.1:n.*5150A>G
ENST00000316418.9:c.*3006A>G (AHRR)	ENSP00000323816.5:n.*3006A>G
NM_001242412.1:c.*3006A>G (AHRR)	NP_001229341.1:n.*3006A>G
NM_020731.4:c.*3006A>G (AHRR)	NP_065782.2:n.*3006A>G
NM_001377236.1:c.*3006A>G (AHRR) MANE Select	NP_001364165.1:n.*3006A>G
NM_001377239.1:c.*3006A>G (AHRR)	NP_001364168.1:n.*3006A>G
NR_165159.2:n.5447A>G (PDCD6-AHRR)
NR_165163.2:n.5393A>G (PDCD6-AHRR)