Canonical Allele Identifier: CA413423080

Gene: AR

Linked Data

• dbSNP Id: rs1230215817
• gnomAD v4: X-67711464-A-C
• MyVariant Identifiers: chrX:g.66931306A>C (hg19) ; chrX:g.67711464A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711464A>C , CM000685.2:g.67711464A>C	GRCh38
NC_000023.10:g.66931306A>C , CM000685.1:g.66931306A>C	GRCh37
NC_000023.9:g.66848031A>C	NCBI36
NG_009014.2:g.172433A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*296A>C	ENSP00000379358.4:n.*296A>C
ENST00000374690.9:c.1948A>C MANE Select	ENSP00000363822.3:p.Thr650Pro
ENST00000396043.3:c.575A>C	ENSP00000379358.3:n.575A>C
ENST00000396044.8:c.1948A>C	ENSP00000379359.3:p.Thr650Pro
ENST00000612452.5:c.1948A>C	ENSP00000484033.2:p.Thr650Pro
ENST00000374690.7:c.1948A>C	ENSP00000363822.3:p.Thr650Pro
ENST00000396043.2:c.352A>C	ENSP00000379358.2:p.Thr118Pro
ENST00000396044.7:c.1948A>C	ENSP00000379359.3:p.Thr650Pro
ENST00000612452.4:c.1378A>C	ENSP00000484033.1:p.Thr460Pro
NM_000044.3:c.1948A>C	NP_000035.2:p.Thr650Pro
NM_001011645.2:c.352A>C	NP_001011645.1:p.Thr118Pro
NM_000044.4:c.1948A>C	NP_000035.2:p.Thr650Pro
NM_001011645.3:c.352A>C	NP_001011645.1:p.Thr118Pro
NM_000044.6:c.1948A>C MANE Select	NP_000035.2:p.Thr650Pro