Canonical Allele Identifier: CA2672992286

Gene: AHRR PDCD6-AHRR

Linked Data

• gnomAD v4: 5-437819-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437819C>A , CM000667.2:g.437819C>A	GRCh38
NC_000005.9:g.437934C>A , CM000667.1:g.437934C>A	GRCh37
NC_000005.8:g.490934C>A	NCBI36
NG_029834.1:g.138644C>A
NG_029834.2:g.138644C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684583.1:c.*2985C>A (AHRR) MANE Select	ENSP00000507476.1:n.*2985C>A
ENST00000316418.10:c.*2985C>A (AHRR)	ENSP00000323816.6:n.*2985C>A
ENST00000505113.6:c.*5075C>A (PDCD6-AHRR)	ENSP00000424601.2:n.*5075C>A
ENST00000675395.1:c.*5129C>A (PDCD6-AHRR)	ENSP00000502570.1:n.*5129C>A
ENST00000316418.9:c.*2985C>A (AHRR)	ENSP00000323816.5:n.*2985C>A
NM_001242412.1:c.*2985C>A (AHRR)	NP_001229341.1:n.*2985C>A
NM_020731.4:c.*2985C>A (AHRR)	NP_065782.2:n.*2985C>A
NM_001377236.1:c.*2985C>A (AHRR) MANE Select	NP_001364165.1:n.*2985C>A
NM_001377239.1:c.*2985C>A (AHRR)	NP_001364168.1:n.*2985C>A
NR_165159.2:n.5426C>A (PDCD6-AHRR)
NR_165163.2:n.5372C>A (PDCD6-AHRR)