Canonical Allele Identifier: CA810916372

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs1256434724
• MyVariant Identifiers: chr5:g.438076C>T (hg19) ; chr5:g.437961C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437961C>T , CM000667.2:g.437961C>T	GRCh38
NC_000005.9:g.438076C>T , CM000667.1:g.438076C>T	GRCh37
NC_000005.8:g.491076C>T	NCBI36
NG_029834.1:g.138786C>T
NG_029834.2:g.138786C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684583.1:c.*3127C>T (AHRR) MANE Select	ENSP00000507476.1:n.*3127C>T
ENST00000316418.10:c.*3127C>T (AHRR)	ENSP00000323816.6:n.*3127C>T
ENST00000505113.6:c.*5217C>T (PDCD6-AHRR)	ENSP00000424601.2:n.*5217C>T
ENST00000675395.1:c.*5271C>T (PDCD6-AHRR)	ENSP00000502570.1:n.*5271C>T
ENST00000316418.9:c.*3127C>T (AHRR)	ENSP00000323816.5:n.*3127C>T
NM_001242412.1:c.*3127C>T (AHRR)	NP_001229341.1:n.*3127C>T
NM_020731.4:c.*3127C>T (AHRR)	NP_065782.2:n.*3127C>T
NM_001377236.1:c.*3127C>T (AHRR) MANE Select	NP_001364165.1:n.*3127C>T
NM_001377239.1:c.*3127C>T (AHRR)	NP_001364168.1:n.*3127C>T
NR_165159.2:n.5568C>T (PDCD6-AHRR)
NR_165163.2:n.5514C>T (PDCD6-AHRR)