Canonical Allele Identifier: CA112846589

Gene: AHRR PDCD6-AHRR

Linked Data

• dbSNP Id: rs1003247203
• MyVariant Identifiers: chr5:g.437925T>G (hg19) ; chr5:g.437810T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.437810T>G , CM000667.2:g.437810T>G	GRCh38
NC_000005.9:g.437925T>G , CM000667.1:g.437925T>G	GRCh37
NC_000005.8:g.490925T>G	NCBI36
NG_029834.1:g.138635T>G
NG_029834.2:g.138635T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684583.1:c.*2976T>G (AHRR) MANE Select	ENSP00000507476.1:n.*2976T>G
ENST00000316418.10:c.*2976T>G (AHRR)	ENSP00000323816.6:n.*2976T>G
ENST00000505113.6:c.*5066T>G (PDCD6-AHRR)	ENSP00000424601.2:n.*5066T>G
ENST00000675395.1:c.*5120T>G (PDCD6-AHRR)	ENSP00000502570.1:n.*5120T>G
ENST00000316418.9:c.*2976T>G (AHRR)	ENSP00000323816.5:n.*2976T>G
NM_001242412.1:c.*2976T>G (AHRR)	NP_001229341.1:n.*2976T>G
NM_020731.4:c.*2976T>G (AHRR)	NP_065782.2:n.*2976T>G
NM_001377236.1:c.*2976T>G (AHRR) MANE Select	NP_001364165.1:n.*2976T>G
NM_001377239.1:c.*2976T>G (AHRR)	NP_001364168.1:n.*2976T>G
NR_165159.2:n.5417T>G (PDCD6-AHRR)
NR_165163.2:n.5363T>G (PDCD6-AHRR)