Canonical Allele Identifier: CA2573158998

Gene: AR

Linked Data

• ClinVar Variation Id: 1394063
• ClinVar RCV Id: RCV001927307
• dbSNP Id: rs2147535489

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721833_67721835dup , CM000685.2:g.67721833_67721835dup	GRCh38
NC_000023.10:g.66941675_66941677dup , CM000685.1:g.66941675_66941677dup	GRCh37
NC_000023.9:g.66858400_66858402dup	NCBI36
NG_009014.2:g.182802_182804dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667_*669dup	ENSP00000379358.4:n.*667_*669dup
ENST00000374690.9:c.2319_2321dup MANE Select	ENSP00000363822.3:p.Tyr774Ter
ENST00000396043.3:c.946_948dup	ENSP00000379358.3:n.946_948dup
ENST00000396044.8:c.2174-1853_2174-1851dup	ENSP00000379359.3:n.2174-1853_2174-1851dup
ENST00000612452.5:c.2319_2321dup	ENSP00000484033.2:p.Tyr774Ter
ENST00000374690.7:c.2319_2321dup	ENSP00000363822.3:p.Tyr774Ter
ENST00000396043.2:c.723_725dup	ENSP00000379358.2:p.Tyr242Ter
ENST00000396044.7:c.2174-1853_2174-1851dup	ENSP00000379359.3:n.2174-1853_2174-1851dup
ENST00000612452.4:c.1749_1751dup	ENSP00000484033.1:p.Tyr584Ter
NM_000044.3:c.2319_2321dup	NP_000035.2:p.Tyr774Ter
NM_001011645.2:c.723_725dup	NP_001011645.1:p.Tyr242Ter
NM_000044.4:c.2319_2321dup	NP_000035.2:p.Tyr774Ter
NM_001011645.3:c.723_725dup	NP_001011645.1:p.Tyr242Ter
NM_000044.6:c.2319_2321dup MANE Select	NP_000035.2:p.Tyr774Ter