Canonical Allele Identifier: CA2695234357

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711474del , CM000685.2:g.67711474del	GRCh38
NC_000023.10:g.66931316del , CM000685.1:g.66931316del	GRCh37
NC_000023.9:g.66848041del	NCBI36
NG_009014.2:g.172443del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*306del	ENSP00000379358.4:n.*306del
ENST00000374690.9:c.1958del MANE Select	ENSP00000363822.3:p.Thr653MetfsTer8
ENST00000396043.3:c.585del	ENSP00000379358.3:n.585del
ENST00000396044.8:c.1958del	ENSP00000379359.3:p.Thr653MetfsTer8
ENST00000612452.5:c.1958del	ENSP00000484033.2:p.Thr653MetfsTer8
ENST00000374690.7:c.1958del	ENSP00000363822.3:p.Thr653MetfsTer8
ENST00000396043.2:c.362del	ENSP00000379358.2:p.Thr121MetfsTer8
ENST00000396044.7:c.1958del	ENSP00000379359.3:p.Thr653MetfsTer8
ENST00000612452.4:c.1388del	ENSP00000484033.1:p.Thr463MetfsTer8
NM_000044.3:c.1958del	NP_000035.2:p.Thr653MetfsTer8
NM_001011645.2:c.362del	NP_001011645.1:p.Thr121MetfsTer8
NM_000044.4:c.1958del	NP_000035.2:p.Thr653MetfsTer8
NM_001011645.3:c.362del	NP_001011645.1:p.Thr121MetfsTer8
NM_000044.6:c.1958del MANE Select	NP_000035.2:p.Thr653MetfsTer8