Canonical Allele Identifier: CA1139667601

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643343_67643344delinsCT , CM000685.2:g.67643343_67643344delinsCT	GRCh38
NC_000023.10:g.66863185_66863186delinsCT , CM000685.1:g.66863185_66863186delinsCT	GRCh37
NC_000023.9:g.66779910_66779911delinsCT	NCBI36
NG_009014.2:g.104312_104313delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*52_*53delinsCT	ENSP00000379358.4:n.*52_*53delinsCT
ENST00000374690.9:c.1704_1705delinsCT MANE Select	ENSP00000363822.3:p.Gly569Trp
ENST00000396043.3:c.331_332delinsCT	ENSP00000379358.3:n.331_332delinsCT
ENST00000396044.8:c.1704_1705delinsCT	ENSP00000379359.3:p.Gly569Trp
ENST00000612452.5:c.1704_1705delinsCT	ENSP00000484033.2:p.Gly569Trp
ENST00000374690.7:c.1704_1705delinsCT	ENSP00000363822.3:p.Gly569Trp
ENST00000396043.2:c.108_109delinsCT	ENSP00000379358.2:p.Gly37Trp
ENST00000396044.7:c.1704_1705delinsCT	ENSP00000379359.3:p.Gly569Trp
ENST00000504326.5:c.1704_1705delinsCT	ENSP00000421155.1:p.Gly569Trp
ENST00000513847.5:n.2031_2032delinsCT
ENST00000514029.5:c.1704_1705delinsCT	ENSP00000425199.1:p.Gly569Trp
ENST00000612010.4:c.1704_1705delinsCT	ENSP00000482407.1:p.Gly569Trp
ENST00000612452.4:c.1134_1135delinsCT	ENSP00000484033.1:p.Gly379Trp
ENST00000613054.2:c.1617-42598_1617-42597delinsCT	ENSP00000479013.1:n.1617-42598_1617-42597delinsCT
NM_000044.3:c.1704_1705delinsCT	NP_000035.2:p.Gly569Trp
NM_001011645.2:c.108_109delinsCT	NP_001011645.1:p.Gly37Trp
NM_000044.4:c.1704_1705delinsCT	NP_000035.2:p.Gly569Trp
NM_001011645.3:c.108_109delinsCT	NP_001011645.1:p.Gly37Trp
NM_001348061.1:c.1704_1705delinsCT	NP_001334990.1:p.Gly569Trp
NM_001348063.1:c.1704_1705delinsCT	NP_001334992.1:p.Gly569Trp
NM_001348064.1:c.1617-42598_1617-42597delinsCT	NP_001334993.1:n.1617-42598_1617-42597delinsCT
NM_000044.6:c.1704_1705delinsCT MANE Select	NP_000035.2:p.Gly569Trp