Canonical Allele Identifier: CA2435065973
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67544824_67544826delinsCTG , CM000685.2:g.67544824_67544826delinsCTG GRCh38
NC_000023.10:g.66764666_66764668delinsCTG , CM000685.1:g.66764666_66764668delinsCTG GRCh37
NC_000023.9:g.66681391_66681393delinsCTG NCBI36
NG_009014.2:g.5793_5795delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.-323_-321delinsCTG ENSP00000379358.4:n.-323_-321delinsCTG
ENST00000374690.9:c.-323_-321delinsCTG MANE Select ENSP00000363822.3:n.-323_-321delinsCTG
ENST00000612452.5:c.-323_-321delinsCTG ENSP00000484033.2:n.-323_-321delinsCTG
ENST00000374690.7:c.-323_-321delinsCTG ENSP00000363822.3:n.-323_-321delinsCTG
ENST00000396044.7:c.-323_-321delinsCTG ENSP00000379359.3:n.-323_-321delinsCTG
ENST00000504326.5:c.-323_-321delinsCTG ENSP00000421155.1:n.-323_-321delinsCTG
ENST00000513847.5:n.5_7delinsCTG
ENST00000514029.5:c.-323_-321delinsCTG ENSP00000425199.1:n.-323_-321delinsCTG
ENST00000612010.4:c.-323_-321delinsCTG ENSP00000482407.1:n.-323_-321delinsCTG
ENST00000612452.4:c.-893_-891delinsCTG ENSP00000484033.1:n.-893_-891delinsCTG
ENST00000613054.2:c.-323_-321delinsCTG ENSP00000479013.1:n.-323_-321delinsCTG
NM_000044.3:c.-323_-321delinsCTG NP_000035.2:n.-323_-321delinsCTG
NM_000044.4:c.-323_-321delinsCTG NP_000035.2:n.-323_-321delinsCTG
NM_001011645.3:c.-2106_-2104delinsCTG NP_001011645.1:n.-2106_-2104delinsCTG
NM_001348061.1:c.-323_-321delinsCTG NP_001334990.1:n.-323_-321delinsCTG
NM_001348063.1:c.-323_-321delinsCTG NP_001334992.1:n.-323_-321delinsCTG
NM_001348064.1:c.-323_-321delinsCTG NP_001334993.1:n.-323_-321delinsCTG
NM_000044.6:c.-323_-321delinsCTG MANE Select NP_000035.2:n.-323_-321delinsCTG