Canonical Allele Identifier: CA120769

Gene: AR

Linked Data

• ClinVar Variation Id: 9842
• ClinVar RCV Id: RCV000010516
• dbSNP Id: rs137852589
• MyVariant Identifiers: chrX:g.66941699G>T (hg19) ; chrX:g.67721857G>T (hg38)
• PubMed: PMID:1307250 ; PMID:8990010 ; PMID:10323251 ; PMID:11549642

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721857G>T , CM000685.2:g.67721857G>T	GRCh38
NC_000023.10:g.66941699G>T , CM000685.1:g.66941699G>T	GRCh37
NC_000023.9:g.66858424G>T	NCBI36
NG_009014.2:g.182826G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*691G>T	ENSP00000379358.4:n.*691G>T
ENST00000374690.9:c.2343G>T MANE Select	ENSP00000363822.3:p.Met781Ile
ENST00000396043.3:c.970G>T	ENSP00000379358.3:n.970G>T
ENST00000396044.8:c.2174-1829G>T	ENSP00000379359.3:n.2174-1829G>T
ENST00000612452.5:c.2343G>T	ENSP00000484033.2:p.Met781Ile
ENST00000374690.7:c.2343G>T	ENSP00000363822.3:p.Met781Ile
ENST00000396043.2:c.747G>T	ENSP00000379358.2:p.Met249Ile
ENST00000396044.7:c.2174-1829G>T	ENSP00000379359.3:n.2174-1829G>T
ENST00000612452.4:c.1773G>T	ENSP00000484033.1:p.Met591Ile
NM_000044.3:c.2343G>T	NP_000035.2:p.Met781Ile
NM_001011645.2:c.747G>T	NP_001011645.1:p.Met249Ile
NM_000044.4:c.2343G>T	NP_000035.2:p.Met781Ile
NM_001011645.3:c.747G>T	NP_001011645.1:p.Met249Ile
NM_000044.6:c.2343G>T MANE Select	NP_000035.2:p.Met781Ile