Canonical Allele Identifier: CA330771339

Gene: AR

Linked Data

• dbSNP Id: rs780406610
• gnomAD v3: X-67711461-A-C
• gnomAD v4: X-67711461-A-C
• MyVariant Identifiers: chrX:g.66931303A>C (hg19) ; chrX:g.67711461A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711461A>C , CM000685.2:g.67711461A>C	GRCh38
NC_000023.10:g.66931303A>C , CM000685.1:g.66931303A>C	GRCh37
NC_000023.9:g.66848028A>C	NCBI36
NG_009014.2:g.172430A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*293A>C	ENSP00000379358.4:n.*293A>C
ENST00000374690.9:c.1945A>C MANE Select	ENSP00000363822.3:p.Thr649Pro
ENST00000396043.3:c.572A>C	ENSP00000379358.3:n.572A>C
ENST00000396044.8:c.1945A>C	ENSP00000379359.3:p.Thr649Pro
ENST00000612452.5:c.1945A>C	ENSP00000484033.2:p.Thr649Pro
ENST00000374690.7:c.1945A>C	ENSP00000363822.3:p.Thr649Pro
ENST00000396043.2:c.349A>C	ENSP00000379358.2:p.Thr117Pro
ENST00000396044.7:c.1945A>C	ENSP00000379359.3:p.Thr649Pro
ENST00000612452.4:c.1375A>C	ENSP00000484033.1:p.Thr459Pro
NM_000044.3:c.1945A>C	NP_000035.2:p.Thr649Pro
NM_001011645.2:c.349A>C	NP_001011645.1:p.Thr117Pro
NM_000044.4:c.1945A>C	NP_000035.2:p.Thr649Pro
NM_001011645.3:c.349A>C	NP_001011645.1:p.Thr117Pro
NM_000044.6:c.1945A>C MANE Select	NP_000035.2:p.Thr649Pro