Canonical Allele Identifier: CA1133892086
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs2076136976

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721810dup , CM000685.2:g.67721810dup GRCh38
NC_000023.10:g.66941652dup , CM000685.1:g.66941652dup GRCh37
NC_000023.9:g.66858377dup NCBI36
NG_009014.2:g.182779dup

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*667-23dup ENSP00000379358.4:n.*667-23dup
ENST00000374690.9:c.2319-23dup MANE Select ENSP00000363822.3:n.2319-23dup
ENST00000396043.3:c.946-23dup ENSP00000379358.3:n.946-23dup
ENST00000396044.8:c.2174-1876dup ENSP00000379359.3:n.2174-1876dup
ENST00000612452.5:c.2319-23dup ENSP00000484033.2:n.2319-23dup
ENST00000374690.7:c.2319-23dup ENSP00000363822.3:n.2319-23dup
ENST00000396043.2:c.723-23dup ENSP00000379358.2:n.723-23dup
ENST00000396044.7:c.2174-1876dup ENSP00000379359.3:n.2174-1876dup
ENST00000612452.4:c.1749-23dup ENSP00000484033.1:n.1749-23dup
NM_000044.3:c.2319-23dup NP_000035.2:n.2319-23dup
NM_001011645.2:c.723-23dup NP_001011645.1:n.723-23dup
NM_000044.4:c.2319-23dup NP_000035.2:n.2319-23dup
NM_001011645.3:c.723-23dup NP_001011645.1:n.723-23dup
NM_000044.6:c.2319-23dup MANE Select NP_000035.2:n.2319-23dup