Canonical Allele Identifier: CA2695234380

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722923del , CM000685.2:g.67722923del	GRCh38
NC_000023.10:g.66942765del , CM000685.1:g.66942765del	GRCh37
NC_000023.9:g.66859490del	NCBI36
NG_009014.2:g.183892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*894del	ENSP00000379358.4:n.*894del
ENST00000374690.9:c.2546del MANE Select	ENSP00000363822.3:p.Asn849IlefsTer?
ENST00000396043.3:c.1173del	ENSP00000379358.3:n.1173del
ENST00000396044.8:c.2174-763del	ENSP00000379359.3:n.2174-763del
ENST00000612452.5:c.2546del	ENSP00000484033.2:p.Asn849IlefsTer?
ENST00000374690.7:c.2546del	ENSP00000363822.3:p.Asn849IlefsTer?
ENST00000396043.2:c.950del	ENSP00000379358.2:p.Asn317IlefsTer?
ENST00000396044.7:c.2174-763del	ENSP00000379359.3:n.2174-763del
ENST00000612452.4:c.1997del	ENSP00000484033.1:p.Asn666IlefsTer?
NM_000044.3:c.2546del	NP_000035.2:p.Asn849IlefsTer?
NM_001011645.2:c.950del	NP_001011645.1:p.Asn317IlefsTer?
NM_000044.4:c.2546del	NP_000035.2:p.Asn849IlefsTer?
NM_001011645.3:c.950del	NP_001011645.1:p.Asn317IlefsTer?
NM_000044.6:c.2546del MANE Select	NP_000035.2:p.Asn849IlefsTer?