Canonical Allele Identifier: CA2693923822
Gene: AR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67544927_67544929dup , CM000685.2:g.67544927_67544929dup GRCh38
NC_000023.10:g.66764769_66764771dup , CM000685.1:g.66764769_66764771dup GRCh37
NC_000023.9:g.66681494_66681496dup NCBI36
NG_009014.2:g.5896_5898dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.-220_-218dup ENSP00000379358.4:n.-220_-218dup
ENST00000374690.9:c.-220_-218dup MANE Select ENSP00000363822.3:n.-220_-218dup
ENST00000612452.5:c.-220_-218dup ENSP00000484033.2:n.-220_-218dup
ENST00000374690.7:c.-220_-218dup ENSP00000363822.3:n.-220_-218dup
ENST00000396044.7:c.-220_-218dup ENSP00000379359.3:n.-220_-218dup
ENST00000504326.5:c.-220_-218dup ENSP00000421155.1:n.-220_-218dup
ENST00000513847.5:n.108_110dup
ENST00000514029.5:c.-220_-218dup ENSP00000425199.1:n.-220_-218dup
ENST00000612010.4:c.-220_-218dup ENSP00000482407.1:n.-220_-218dup
ENST00000612452.4:c.-790_-788dup ENSP00000484033.1:n.-790_-788dup
ENST00000613054.2:c.-220_-218dup ENSP00000479013.1:n.-220_-218dup
NM_000044.3:c.-220_-218dup NP_000035.2:n.-220_-218dup
NM_000044.4:c.-220_-218dup NP_000035.2:n.-220_-218dup
NM_001011645.3:c.-2003_-2001dup NP_001011645.1:n.-2003_-2001dup
NM_001348061.1:c.-220_-218dup NP_001334990.1:n.-220_-218dup
NM_001348063.1:c.-220_-218dup NP_001334992.1:n.-220_-218dup
NM_001348064.1:c.-220_-218dup NP_001334993.1:n.-220_-218dup
NM_000044.6:c.-220_-218dup MANE Select NP_000035.2:n.-220_-218dup