Canonical Allele Identifier: CA112846928

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs543104431
• gnomAD v3: 5-438055-G-A
• gnomAD v4: 5-438055-G-A
• MyVariant Identifiers: chr5:g.438170G>A (hg19) ; chr5:g.438055G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.438055G>A , CM000667.2:g.438055G>A	GRCh38
NC_000005.9:g.438170G>A , CM000667.1:g.438170G>A	GRCh37
NC_000005.8:g.491170G>A	NCBI36
NG_029834.1:g.138880G>A
NG_029834.2:g.138880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684583.1:c.*3221G>A (AHRR) MANE Select	ENSP00000507476.1:n.*3221G>A
ENST00000316418.10:c.*3221G>A (AHRR)	ENSP00000323816.6:n.*3221G>A
ENST00000505113.6:c.*5311G>A (PDCD6-AHRR)	ENSP00000424601.2:n.*5311G>A
ENST00000675395.1:c.*5365G>A (PDCD6-AHRR)	ENSP00000502570.1:n.*5365G>A
ENST00000316418.9:c.*3221G>A (AHRR)	ENSP00000323816.5:n.*3221G>A
NM_001242412.1:c.*3221G>A (AHRR)	NP_001229341.1:n.*3221G>A
NM_020731.4:c.*3221G>A (AHRR)	NP_065782.2:n.*3221G>A
NM_001377236.1:c.*3221G>A (AHRR) MANE Select	NP_001364165.1:n.*3221G>A
NM_001377239.1:c.*3221G>A (AHRR)	NP_001364168.1:n.*3221G>A
NR_165159.2:n.5662G>A (PDCD6-AHRR)
NR_165163.2:n.5608G>A (PDCD6-AHRR)