Canonical Allele Identifier: CA413424536

Gene: AR

Linked Data

• ClinVar Variation Id: 429837
• ClinVar RCV Id: RCV000494389
• dbSNP Id: rs1131691625
• MyVariant Identifiers: chrX:g.66937374T>A (hg19) ; chrX:g.67717532T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717532T>A , CM000685.2:g.67717532T>A	GRCh38
NC_000023.10:g.66937374T>A , CM000685.1:g.66937374T>A	GRCh37
NC_000023.9:g.66854099T>A	NCBI36
NG_009014.2:g.178501T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*576T>A	ENSP00000379358.4:n.*576T>A
ENST00000374690.9:c.2228T>A MANE Select	ENSP00000363822.3:p.Met743Lys
ENST00000396043.3:c.855T>A	ENSP00000379358.3:n.855T>A
ENST00000396044.8:c.2173+5843T>A	ENSP00000379359.3:n.2173+5843T>A
ENST00000612452.5:c.2228T>A	ENSP00000484033.2:p.Met743Lys
ENST00000374690.7:c.2228T>A	ENSP00000363822.3:p.Met743Lys
ENST00000396043.2:c.632T>A	ENSP00000379358.2:p.Met211Lys
ENST00000396044.7:c.2173+5843T>A	ENSP00000379359.3:n.2173+5843T>A
ENST00000612452.4:c.1658T>A	ENSP00000484033.1:p.Met553Lys
NM_000044.3:c.2228T>A	NP_000035.2:p.Met743Lys
NM_001011645.2:c.632T>A	NP_001011645.1:p.Met211Lys
NM_000044.4:c.2228T>A	NP_000035.2:p.Met743Lys
NM_001011645.3:c.632T>A	NP_001011645.1:p.Met211Lys
NM_000044.6:c.2228T>A MANE Select	NP_000035.2:p.Met743Lys