Canonical Allele Identifier: CA1522092536

Gene: AHRR PDCD6-AHRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.428121C= , CM000667.2:g.428121C=	GRCh38
NC_000005.9:g.428236C= , CM000667.1:g.428236C=	GRCh37
NC_000005.8:g.481236C=	NCBI36
NG_029834.1:g.128946C=
NG_029834.2:g.128946C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684583.1:c.908+115C= (AHRR) MANE Select	ENSP00000507476.1:n.908+115C=
ENST00000316418.10:c.908+115C= (AHRR)	ENSP00000323816.6:n.908+115C=
ENST00000505113.6:c.*904+115C= (PDCD6-AHRR)	ENSP00000424601.2:n.*904+115C=
ENST00000512529.6:n.667+115C= (PDCD6-AHRR)
ENST00000675395.1:c.*958+115C= (PDCD6-AHRR)	ENSP00000502570.1:n.*958+115C=
ENST00000316418.9:c.974+115C= (AHRR)	ENSP00000323816.5:n.974+115C=
ENST00000505113.5:c.920+115C= (AHRR)	ENSP00000424601.1:n.920+115C=
ENST00000506456.1:c.488+115C= (AHRR)	ENSP00000426932.1:n.488+115C=
ENST00000511487.1:c.89+115C= (AHRR)	ENSP00000426076.1:n.89+115C=
ENST00000512529.5:c.458+115C= (AHRR)	ENSP00000424880.1:n.458+115C=
NM_001242412.1:c.920+115C= (AHRR)	NP_001229341.1:n.920+115C=
NM_020731.4:c.974+115C= (AHRR)	NP_065782.2:n.974+115C=
NM_001377236.1:c.908+115C= (AHRR) MANE Select	NP_001364165.1:n.908+115C=
NM_001377239.1:c.908+115C= (AHRR)	NP_001364168.1:n.908+115C=
NR_165159.2:n.1255+115C= (PDCD6-AHRR)
NR_165163.2:n.1201+115C= (PDCD6-AHRR)