Canonical Allele Identifier: CA413426458

Gene: AR

Linked Data

• dbSNP Id: rs2147535619
• MyVariant Identifiers: chrX:g.66941697A>G (hg19) ; chrX:g.67721855A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721855A>G , CM000685.2:g.67721855A>G	GRCh38
NC_000023.10:g.66941697A>G , CM000685.1:g.66941697A>G	GRCh37
NC_000023.9:g.66858422A>G	NCBI36
NG_009014.2:g.182824A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*689A>G	ENSP00000379358.4:n.*689A>G
ENST00000374690.9:c.2341A>G MANE Select	ENSP00000363822.3:p.Met781Val
ENST00000396043.3:c.968A>G	ENSP00000379358.3:n.968A>G
ENST00000396044.8:c.2174-1831A>G	ENSP00000379359.3:n.2174-1831A>G
ENST00000612452.5:c.2341A>G	ENSP00000484033.2:p.Met781Val
ENST00000374690.7:c.2341A>G	ENSP00000363822.3:p.Met781Val
ENST00000396043.2:c.745A>G	ENSP00000379358.2:p.Met249Val
ENST00000396044.7:c.2174-1831A>G	ENSP00000379359.3:n.2174-1831A>G
ENST00000612452.4:c.1771A>G	ENSP00000484033.1:p.Met591Val
NM_000044.3:c.2341A>G	NP_000035.2:p.Met781Val
NM_001011645.2:c.745A>G	NP_001011645.1:p.Met249Val
NM_000044.4:c.2341A>G	NP_000035.2:p.Met781Val
NM_001011645.3:c.745A>G	NP_001011645.1:p.Met249Val
NM_000044.6:c.2341A>G MANE Select	NP_000035.2:p.Met781Val