Canonical Allele Identifier: CA2695234339

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643291_67643298dup , CM000685.2:g.67643291_67643298dup	GRCh38
NC_000023.10:g.66863133_66863140dup , CM000685.1:g.66863133_66863140dup	GRCh37
NC_000023.9:g.66779858_66779865dup	NCBI36
NG_009014.2:g.104260_104267dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.1839_*7dup	ENSP00000379358.4:n.1839_*7dup
ENST00000374690.9:c.1652_1659dup MANE Select	ENSP00000363822.3:p.Phe554ThrfsTer11
ENST00000396043.3:c.279_286dup	ENSP00000379358.3:n.279_286dup
ENST00000396044.8:c.1652_1659dup	ENSP00000379359.3:p.Phe554ThrfsTer11
ENST00000612452.5:c.1652_1659dup	ENSP00000484033.2:p.Phe554ThrfsTer11
ENST00000374690.7:c.1652_1659dup	ENSP00000363822.3:p.Phe554ThrfsTer11
ENST00000396043.2:c.56_63dup	ENSP00000379358.2:p.Phe22ThrfsTer11
ENST00000396044.7:c.1652_1659dup	ENSP00000379359.3:p.Phe554ThrfsTer11
ENST00000504326.5:c.1652_1659dup	ENSP00000421155.1:p.Phe554ThrfsTer11
ENST00000513847.5:n.1979_1986dup
ENST00000514029.5:c.1652_1659dup	ENSP00000425199.1:p.Phe554ThrfsTer11
ENST00000612010.4:c.1652_1659dup	ENSP00000482407.1:p.Phe554ThrfsTer11
ENST00000612452.4:c.1082_1089dup	ENSP00000484033.1:p.Phe364ThrfsTer11
ENST00000613054.2:c.1617-42650_1617-42643dup	ENSP00000479013.1:n.1617-42650_1617-42643...
NM_000044.3:c.1652_1659dup	NP_000035.2:p.Phe554ThrfsTer11
NM_001011645.2:c.56_63dup	NP_001011645.1:p.Phe22ThrfsTer11
NM_000044.4:c.1652_1659dup	NP_000035.2:p.Phe554ThrfsTer11
NM_001011645.3:c.56_63dup	NP_001011645.1:p.Phe22ThrfsTer11
NM_001348061.1:c.1652_1659dup	NP_001334990.1:p.Phe554ThrfsTer11
NM_001348063.1:c.1652_1659dup	NP_001334992.1:p.Phe554ThrfsTer11
NM_001348064.1:c.1617-42650_1617-42643dup	NP_001334993.1:n.1617-42650_1617-42643dup...
NM_000044.6:c.1652_1659dup MANE Select	NP_000035.2:p.Phe554ThrfsTer11