Canonical Allele Identifier: CA413422971

Gene: AR

Linked Data

• gnomAD v4: X-67711414-A-C
• MyVariant Identifiers: chrX:g.66931256A>C (hg19) ; chrX:g.67711414A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711414A>C , CM000685.2:g.67711414A>C	GRCh38
NC_000023.10:g.66931256A>C , CM000685.1:g.66931256A>C	GRCh37
NC_000023.9:g.66847981A>C	NCBI36
NG_009014.2:g.172383A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*246A>C	ENSP00000379358.4:n.*246A>C
ENST00000374690.9:c.1898A>C MANE Select	ENSP00000363822.3:p.Lys633Thr
ENST00000396043.3:c.525A>C	ENSP00000379358.3:n.525A>C
ENST00000396044.8:c.1898A>C	ENSP00000379359.3:p.Lys633Thr
ENST00000612452.5:c.1898A>C	ENSP00000484033.2:p.Lys633Thr
ENST00000374690.7:c.1898A>C	ENSP00000363822.3:p.Lys633Thr
ENST00000396043.2:c.302A>C	ENSP00000379358.2:p.Lys101Thr
ENST00000396044.7:c.1898A>C	ENSP00000379359.3:p.Lys633Thr
ENST00000612452.4:c.1328A>C	ENSP00000484033.1:p.Lys443Thr
NM_000044.3:c.1898A>C	NP_000035.2:p.Lys633Thr
NM_001011645.2:c.302A>C	NP_001011645.1:p.Lys101Thr
NM_000044.4:c.1898A>C	NP_000035.2:p.Lys633Thr
NM_001011645.3:c.302A>C	NP_001011645.1:p.Lys101Thr
NM_000044.6:c.1898A>C MANE Select	NP_000035.2:p.Lys633Thr