Canonical Allele Identifier: CA2740092168

Gene: AR

Linked Data

• ClinVar Variation Id: 2947606
• ClinVar RCV Id: RCV003804236

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545692dup , CM000685.2:g.67545692dup	GRCh38
NC_000023.10:g.66765534dup , CM000685.1:g.66765534dup	GRCh37
NC_000023.9:g.66682259dup	NCBI36
NG_009014.2:g.6661dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.546dup	ENSP00000379358.4:p.Asp183ArgfsTer?
ENST00000374690.9:c.546dup MANE Select	ENSP00000363822.3:p.Asp183ArgfsTer?
ENST00000396044.8:c.546dup	ENSP00000379359.3:p.Asp183ArgfsTer?
ENST00000612452.5:c.546dup	ENSP00000484033.2:p.Asp183ArgfsTer?
ENST00000374690.7:c.546dup	ENSP00000363822.3:p.Asp183ArgfsTer?
ENST00000396044.7:c.546dup	ENSP00000379359.3:p.Asp183ArgfsTer?
ENST00000504326.5:c.546dup	ENSP00000421155.1:p.Asp183ArgfsTer?
ENST00000513847.5:n.873dup
ENST00000514029.5:c.546dup	ENSP00000425199.1:p.Asp183ArgfsTer?
ENST00000612010.4:c.546dup	ENSP00000482407.1:p.Asp183ArgfsTer?
ENST00000612452.4:c.-25dup	ENSP00000484033.1:n.-25dup
ENST00000613054.2:c.546dup	ENSP00000479013.1:p.Asp183ArgfsTer?
NM_000044.3:c.546dup	NP_000035.2:p.Asp183ArgfsTer?
NM_000044.4:c.546dup	NP_000035.2:p.Asp183ArgfsTer?
NM_001011645.3:c.-1238dup	NP_001011645.1:n.-1238dup
NM_001348061.1:c.546dup	NP_001334990.1:p.Asp183ArgfsTer?
NM_001348063.1:c.546dup	NP_001334992.1:p.Asp183ArgfsTer?
NM_001348064.1:c.546dup	NP_001334993.1:p.Asp183ArgfsTer?
NM_000044.6:c.546dup MANE Select	NP_000035.2:p.Asp183ArgfsTer?