Canonical Allele Identifier: CA1522097543

Gene: AHRR PDCD6-AHRR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437977_437978delinsGT , CM000667.2:g.437977_437978delinsGT	GRCh38
NC_000005.9:g.438092_438093delinsGT , CM000667.1:g.438092_438093delinsGT	GRCh37
NC_000005.8:g.491092_491093delinsGT	NCBI36
NG_029834.1:g.138802_138803delinsGT
NG_029834.2:g.138802_138803delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684583.1:c.*3143_*3144delinsGT (AHRR) MANE Select	ENSP00000507476.1:n.*3143_*3144delinsGT
ENST00000316418.10:c.*3143_*3144delinsGT (AHRR)	ENSP00000323816.6:n.*3143_*3144delinsGT
ENST00000505113.6:c.*5233_*5234delinsGT (PDCD6-AHRR)	ENSP00000424601.2:n.*5233_*5234delinsGT
ENST00000675395.1:c.*5287_*5288delinsGT (PDCD6-AHRR)	ENSP00000502570.1:n.*5287_*5288delinsGT
ENST00000316418.9:c.*3143_*3144delinsGT (AHRR)	ENSP00000323816.5:n.*3143_*3144delinsGT
NM_001242412.1:c.*3143_*3144delinsGT (AHRR)	NP_001229341.1:n.*3143_*3144delinsGT
NM_020731.4:c.*3143_*3144delinsGT (AHRR)	NP_065782.2:n.*3143_*3144delinsGT
NM_001377236.1:c.*3143_*3144delinsGT (AHRR) MANE Select	NP_001364165.1:n.*3143_*3144delinsGT
NM_001377239.1:c.*3143_*3144delinsGT (AHRR)	NP_001364168.1:n.*3143_*3144delinsGT
NR_165159.2:n.5584_5585delinsGT (PDCD6-AHRR)
NR_165163.2:n.5530_5531delinsGT (PDCD6-AHRR)