Canonical Allele Identifier: CA2695234350

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686088_67686090del , CM000685.2:g.67686088_67686090del	GRCh38
NC_000023.10:g.66905930_66905932del , CM000685.1:g.66905930_66905932del	GRCh37
NC_000023.9:g.66822655_66822657del	NCBI36
NG_009014.2:g.147057_147059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*195_*197del	ENSP00000379358.4:n.*195_*197del
ENST00000374690.9:c.1847_1849del MANE Select	ENSP00000363822.3:p.Arg616del
ENST00000396043.3:c.474_476del	ENSP00000379358.3:n.474_476del
ENST00000396044.8:c.1847_1849del	ENSP00000379359.3:p.Arg616del
ENST00000612452.5:c.1847_1849del	ENSP00000484033.2:p.Arg616del
ENST00000374690.7:c.1847_1849del	ENSP00000363822.3:p.Arg616del
ENST00000396043.2:c.251_253del	ENSP00000379358.2:p.Arg84del
ENST00000396044.7:c.1847_1849del	ENSP00000379359.3:p.Arg616del
ENST00000504326.5:c.1847_1849del	ENSP00000421155.1:p.Arg616del
ENST00000513847.5:n.2174_2176del
ENST00000514029.5:c.*328_*330del	ENSP00000425199.1:n.*328_*330del
ENST00000612010.4:c.*199_*201del	ENSP00000482407.1:n.*199_*201del
ENST00000612452.4:c.1277_1279del	ENSP00000484033.1:p.Arg426del
ENST00000613054.2:c.*45_*47del	ENSP00000479013.1:n.*45_*47del
NM_000044.3:c.1847_1849del	NP_000035.2:p.Arg616del
NM_001011645.2:c.251_253del	NP_001011645.1:p.Arg84del
NM_000044.4:c.1847_1849del	NP_000035.2:p.Arg616del
NM_001011645.3:c.251_253del	NP_001011645.1:p.Arg84del
NM_001348061.1:c.1847_1849del	NP_001334990.1:p.Arg616del
NM_001348063.1:c.1847_1849del	NP_001334992.1:p.Arg616del
NM_001348064.1:c.*45_*47del	NP_001334993.1:n.*45_*47del
NM_000044.6:c.1847_1849del MANE Select	NP_000035.2:p.Arg616del