Canonical Allele Identifier: CA413429299

Gene: AR

Linked Data

• ClinVar Variation Id: 653501
• ClinVar RCV Id: RCV000809289
• dbSNP Id: rs1602255415
• MyVariant Identifiers: chrX:g.66905927G>C (hg19) ; chrX:g.67686085G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686085G>C , CM000685.2:g.67686085G>C	GRCh38
NC_000023.10:g.66905927G>C , CM000685.1:g.66905927G>C	GRCh37
NC_000023.9:g.66822652G>C	NCBI36
NG_009014.2:g.147054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*192G>C	ENSP00000379358.4:n.*192G>C
ENST00000374690.9:c.1844G>C MANE Select	ENSP00000363822.3:p.Cys615Ser
ENST00000396043.3:c.471G>C	ENSP00000379358.3:n.471G>C
ENST00000396044.8:c.1844G>C	ENSP00000379359.3:p.Cys615Ser
ENST00000612452.5:c.1844G>C	ENSP00000484033.2:p.Cys615Ser
ENST00000374690.7:c.1844G>C	ENSP00000363822.3:p.Cys615Ser
ENST00000396043.2:c.248G>C	ENSP00000379358.2:p.Cys83Ser
ENST00000396044.7:c.1844G>C	ENSP00000379359.3:p.Cys615Ser
ENST00000504326.5:c.1844G>C	ENSP00000421155.1:p.Cys615Ser
ENST00000513847.5:n.2171G>C
ENST00000514029.5:c.*325G>C	ENSP00000425199.1:n.*325G>C
ENST00000612010.4:c.*196G>C	ENSP00000482407.1:n.*196G>C
ENST00000612452.4:c.1274G>C	ENSP00000484033.1:p.Cys425Ser
ENST00000613054.2:c.*42G>C	ENSP00000479013.1:n.*42G>C
NM_000044.3:c.1844G>C	NP_000035.2:p.Cys615Ser
NM_001011645.2:c.248G>C	NP_001011645.1:p.Cys83Ser
NM_000044.4:c.1844G>C	NP_000035.2:p.Cys615Ser
NM_001011645.3:c.248G>C	NP_001011645.1:p.Cys83Ser
NM_001348061.1:c.1844G>C	NP_001334990.1:p.Cys615Ser
NM_001348063.1:c.1844G>C	NP_001334992.1:p.Cys615Ser
NM_001348064.1:c.*42G>C	NP_001334993.1:n.*42G>C
NM_000044.6:c.1844G>C MANE Select	NP_000035.2:p.Cys615Ser