Canonical Allele Identifier: CA2738701178

Gene: AR

Linked Data

• dbSNP Id: rs2147498079

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686160_67686164del , CM000685.2:g.67686160_67686164del	GRCh38
NC_000023.10:g.66906002_66906006del , CM000685.1:g.66906002_66906006del	GRCh37
NC_000023.9:g.66822727_66822731del	NCBI36
NG_009014.2:g.147129_147133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*233+34_*233+38del	ENSP00000379358.4:n.*233+34_*233+38del
ENST00000374690.9:c.1885+34_1885+38del MANE Select	ENSP00000363822.3:n.1885+34_1885+38del
ENST00000396043.3:c.512+34_512+38del	ENSP00000379358.3:n.512+34_512+38del
ENST00000396044.8:c.1885+34_1885+38del	ENSP00000379359.3:n.1885+34_1885+38del
ENST00000612452.5:c.1885+34_1885+38del	ENSP00000484033.2:n.1885+34_1885+38del
ENST00000374690.7:c.1885+34_1885+38del	ENSP00000363822.3:n.1885+34_1885+38del
ENST00000396043.2:c.289+34_289+38del	ENSP00000379358.2:n.289+34_289+38del
ENST00000396044.7:c.1885+34_1885+38del	ENSP00000379359.3:n.1885+34_1885+38del
ENST00000504326.5:c.1885+34_1885+38del	ENSP00000421155.1:n.1885+34_1885+38del
ENST00000513847.5:n.2212+34_2212+38del
ENST00000514029.5:c.*366+34_*366+38del	ENSP00000425199.1:n.*366+34_*366+38del
ENST00000612010.4:c.*237+34_*237+38del	ENSP00000482407.1:n.*237+34_*237+38del
ENST00000612452.4:c.1315+34_1315+38del	ENSP00000484033.1:n.1315+34_1315+38del
ENST00000613054.2:c.*83+34_*83+38del	ENSP00000479013.1:n.*83+34_*83+38del
NM_000044.3:c.1885+34_1885+38del	NP_000035.2:n.1885+34_1885+38del
NM_001011645.2:c.289+34_289+38del	NP_001011645.1:n.289+34_289+38del
NM_000044.4:c.1885+34_1885+38del	NP_000035.2:n.1885+34_1885+38del
NM_001011645.3:c.289+34_289+38del	NP_001011645.1:n.289+34_289+38del
NM_001348061.1:c.1885+34_1885+38del	NP_001334990.1:n.1885+34_1885+38del
NM_001348063.1:c.1885+34_1885+38del	NP_001334992.1:n.1885+34_1885+38del
NM_001348064.1:c.*83+34_*83+38del	NP_001334993.1:n.*83+34_*83+38del
NM_000044.6:c.1885+34_1885+38del MANE Select	NP_000035.2:n.1885+34_1885+38del