Canonical Allele Identifier: CA877566065

Gene: AR

Linked Data

• dbSNP Id: rs1464871537
• MyVariant Identifiers: chrX:g.66941600_66941601insA (hg19) ; chrX:g.67721758_67721759insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721760dup , CM000685.2:g.67721760dup	GRCh38
NC_000023.10:g.66941602dup , CM000685.1:g.66941602dup	GRCh37
NC_000023.9:g.66858327dup	NCBI36
NG_009014.2:g.182729dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667-73dup	ENSP00000379358.4:n.*667-73dup
ENST00000374690.9:c.2319-73dup MANE Select	ENSP00000363822.3:n.2319-73dup
ENST00000396043.3:c.946-73dup	ENSP00000379358.3:n.946-73dup
ENST00000396044.8:c.2174-1926dup	ENSP00000379359.3:n.2174-1926dup
ENST00000612452.5:c.2319-73dup	ENSP00000484033.2:n.2319-73dup
ENST00000374690.7:c.2319-73dup	ENSP00000363822.3:n.2319-73dup
ENST00000396043.2:c.723-73dup	ENSP00000379358.2:n.723-73dup
ENST00000396044.7:c.2174-1926dup	ENSP00000379359.3:n.2174-1926dup
ENST00000612452.4:c.1749-73dup	ENSP00000484033.1:n.1749-73dup
NM_000044.3:c.2319-73dup	NP_000035.2:n.2319-73dup
NM_001011645.2:c.723-73dup	NP_001011645.1:n.723-73dup
NM_000044.4:c.2319-73dup	NP_000035.2:n.2319-73dup
NM_001011645.3:c.723-73dup	NP_001011645.1:n.723-73dup
NM_000044.6:c.2319-73dup MANE Select	NP_000035.2:n.2319-73dup