Canonical Allele Identifier: CA1072388310

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs1737167284
• gnomAD v3: 5-437978-T-A
• gnomAD v4: 5-437978-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437978T>A , CM000667.2:g.437978T>A	GRCh38
NC_000005.9:g.438093T>A , CM000667.1:g.438093T>A	GRCh37
NC_000005.8:g.491093T>A	NCBI36
NG_029834.1:g.138803T>A
NG_029834.2:g.138803T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684583.1:c.*3144T>A (AHRR) MANE Select	ENSP00000507476.1:n.*3144T>A
ENST00000316418.10:c.*3144T>A (AHRR)	ENSP00000323816.6:n.*3144T>A
ENST00000505113.6:c.*5234T>A (PDCD6-AHRR)	ENSP00000424601.2:n.*5234T>A
ENST00000675395.1:c.*5288T>A (PDCD6-AHRR)	ENSP00000502570.1:n.*5288T>A
ENST00000316418.9:c.*3144T>A (AHRR)	ENSP00000323816.5:n.*3144T>A
NM_001242412.1:c.*3144T>A (AHRR)	NP_001229341.1:n.*3144T>A
NM_020731.4:c.*3144T>A (AHRR)	NP_065782.2:n.*3144T>A
NM_001377236.1:c.*3144T>A (AHRR) MANE Select	NP_001364165.1:n.*3144T>A
NM_001377239.1:c.*3144T>A (AHRR)	NP_001364168.1:n.*3144T>A
NR_165159.2:n.5585T>A (PDCD6-AHRR)
NR_165163.2:n.5531T>A (PDCD6-AHRR)