Canonical Allele Identifier: CA413423445

Gene: AR

Linked Data

• dbSNP Id: rs2147525104
• MyVariant Identifiers: chrX:g.66931472T>C (hg19) ; chrX:g.67711630T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711630T>C , CM000685.2:g.67711630T>C	GRCh38
NC_000023.10:g.66931472T>C , CM000685.1:g.66931472T>C	GRCh37
NC_000023.9:g.66848197T>C	NCBI36
NG_009014.2:g.172599T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*462T>C	ENSP00000379358.4:n.*462T>C
ENST00000374690.9:c.2114T>C MANE Select	ENSP00000363822.3:p.Leu705Pro
ENST00000396043.3:c.741T>C	ENSP00000379358.3:n.741T>C
ENST00000396044.8:c.2114T>C	ENSP00000379359.3:p.Leu705Pro
ENST00000612452.5:c.2114T>C	ENSP00000484033.2:p.Leu705Pro
ENST00000374690.7:c.2114T>C	ENSP00000363822.3:p.Leu705Pro
ENST00000396043.2:c.518T>C	ENSP00000379358.2:p.Leu173Pro
ENST00000396044.7:c.2114T>C	ENSP00000379359.3:p.Leu705Pro
ENST00000612452.4:c.1544T>C	ENSP00000484033.1:p.Leu515Pro
NM_000044.3:c.2114T>C	NP_000035.2:p.Leu705Pro
NM_001011645.2:c.518T>C	NP_001011645.1:p.Leu173Pro
NM_000044.4:c.2114T>C	NP_000035.2:p.Leu705Pro
NM_001011645.3:c.518T>C	NP_001011645.1:p.Leu173Pro
NM_000044.6:c.2114T>C MANE Select	NP_000035.2:p.Leu705Pro