Canonical Allele Identifier: CA413424646

Gene: AR

Linked Data

• ClinVar Variation Id: 426560
• ClinVar RCV Id: RCV003766746
• dbSNP Id: rs1085307685
• MyVariant Identifiers: chrX:g.66937394A>G (hg19) ; chrX:g.67717552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717552A>G , CM000685.2:g.67717552A>G	GRCh38
NC_000023.10:g.66937394A>G , CM000685.1:g.66937394A>G	GRCh37
NC_000023.9:g.66854119A>G	NCBI36
NG_009014.2:g.178521A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*596A>G	ENSP00000379358.4:n.*596A>G
ENST00000374690.9:c.2248A>G MANE Select	ENSP00000363822.3:p.Met750Val
ENST00000396043.3:c.875A>G	ENSP00000379358.3:n.875A>G
ENST00000396044.8:c.2173+5863A>G	ENSP00000379359.3:n.2173+5863A>G
ENST00000612452.5:c.2248A>G	ENSP00000484033.2:p.Met750Val
ENST00000374690.7:c.2248A>G	ENSP00000363822.3:p.Met750Val
ENST00000396043.2:c.652A>G	ENSP00000379358.2:p.Met218Val
ENST00000396044.7:c.2173+5863A>G	ENSP00000379359.3:n.2173+5863A>G
ENST00000612452.4:c.1678A>G	ENSP00000484033.1:p.Met560Val
NM_000044.3:c.2248A>G	NP_000035.2:p.Met750Val
NM_001011645.2:c.652A>G	NP_001011645.1:p.Met218Val
NM_000044.4:c.2248A>G	NP_000035.2:p.Met750Val
NM_001011645.3:c.652A>G	NP_001011645.1:p.Met218Val
NM_000044.6:c.2248A>G MANE Select	NP_000035.2:p.Met750Val