Canonical Allele Identifier: CA516973470

Gene: AR

Linked Data

• ClinVar Variation Id: 2927461
• ClinVar RCV Id: RCV003784091
• dbSNP Id: rs2075964847
• gnomAD v4: X-67686065-A-C
• MyVariant Identifiers: chrX:g.66905907A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686065A>C , CM000685.2:g.67686065A>C	GRCh38
NC_000023.10:g.66905907A>C , CM000685.1:g.66905907A>C	GRCh37
NC_000023.9:g.66822632A>C	NCBI36
NG_009014.2:g.147034A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*172A>C	ENSP00000379358.4:n.*172A>C
ENST00000374690.9:c.1824A>C MANE Select	ENSP00000363822.3:p.Arg608=
ENST00000396043.3:c.451A>C	ENSP00000379358.3:n.451A>C
ENST00000396044.8:c.1824A>C	ENSP00000379359.3:p.Arg608=
ENST00000612452.5:c.1824A>C	ENSP00000484033.2:p.Arg608=
ENST00000374690.7:c.1824A>C	ENSP00000363822.3:p.Arg608=
ENST00000396043.2:c.228A>C	ENSP00000379358.2:p.Arg76=
ENST00000396044.7:c.1824A>C	ENSP00000379359.3:p.Arg608=
ENST00000504326.5:c.1824A>C	ENSP00000421155.1:p.Arg608=
ENST00000513847.5:n.2151A>C
ENST00000514029.5:c.*305A>C	ENSP00000425199.1:n.*305A>C
ENST00000612010.4:c.*176A>C	ENSP00000482407.1:n.*176A>C
ENST00000612452.4:c.1254A>C	ENSP00000484033.1:p.Arg418=
ENST00000613054.2:c.*22A>C	ENSP00000479013.1:n.*22A>C
NM_000044.3:c.1824A>C	NP_000035.2:p.Arg608=
NM_001011645.2:c.228A>C	NP_001011645.1:p.Arg76=
NM_000044.4:c.1824A>C	NP_000035.2:p.Arg608=
NM_001011645.3:c.228A>C	NP_001011645.1:p.Arg76=
NM_001348061.1:c.1824A>C	NP_001334990.1:p.Arg608=
NM_001348063.1:c.1824A>C	NP_001334992.1:p.Arg608=
NM_001348064.1:c.*22A>C	NP_001334993.1:n.*22A>C
NM_000044.6:c.1824A>C MANE Select	NP_000035.2:p.Arg608=