Canonical Allele Identifier: CA413424534

Gene: AR

Linked Data

• ClinVar Variation Id: 1339111
• ClinVar RCV Id: RCV001823565
• dbSNP Id: rs2147530802
• MyVariant Identifiers: chrX:g.66937373A>G (hg19) ; chrX:g.67717531A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717531A>G , CM000685.2:g.67717531A>G	GRCh38
NC_000023.10:g.66937373A>G , CM000685.1:g.66937373A>G	GRCh37
NC_000023.9:g.66854098A>G	NCBI36
NG_009014.2:g.178500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*575A>G	ENSP00000379358.4:n.*575A>G
ENST00000374690.9:c.2227A>G MANE Select	ENSP00000363822.3:p.Met743Val
ENST00000396043.3:c.854A>G	ENSP00000379358.3:n.854A>G
ENST00000396044.8:c.2173+5842A>G	ENSP00000379359.3:n.2173+5842A>G
ENST00000612452.5:c.2227A>G	ENSP00000484033.2:p.Met743Val
ENST00000374690.7:c.2227A>G	ENSP00000363822.3:p.Met743Val
ENST00000396043.2:c.631A>G	ENSP00000379358.2:p.Met211Val
ENST00000396044.7:c.2173+5842A>G	ENSP00000379359.3:n.2173+5842A>G
ENST00000612452.4:c.1657A>G	ENSP00000484033.1:p.Met553Val
NM_000044.3:c.2227A>G	NP_000035.2:p.Met743Val
NM_001011645.2:c.631A>G	NP_001011645.1:p.Met211Val
NM_000044.4:c.2227A>G	NP_000035.2:p.Met743Val
NM_001011645.3:c.631A>G	NP_001011645.1:p.Met211Val
NM_000044.6:c.2227A>G MANE Select	NP_000035.2:p.Met743Val