Canonical Allele Identifier: CA2738701080

Gene: AR

Linked Data

• ClinVar Variation Id: 2924300
• ClinVar RCV Id: RCV003786050
• dbSNP Id: rs2147498027

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686140C>G , CM000685.2:g.67686140C>G	GRCh38
NC_000023.10:g.66905982C>G , CM000685.1:g.66905982C>G	GRCh37
NC_000023.9:g.66822707C>G	NCBI36
NG_009014.2:g.147109C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*233+14C>G	ENSP00000379358.4:n.*233+14C>G
ENST00000374690.9:c.1885+14C>G MANE Select	ENSP00000363822.3:n.1885+14C>G
ENST00000396043.3:c.512+14C>G	ENSP00000379358.3:n.512+14C>G
ENST00000396044.8:c.1885+14C>G	ENSP00000379359.3:n.1885+14C>G
ENST00000612452.5:c.1885+14C>G	ENSP00000484033.2:n.1885+14C>G
ENST00000374690.7:c.1885+14C>G	ENSP00000363822.3:n.1885+14C>G
ENST00000396043.2:c.289+14C>G	ENSP00000379358.2:n.289+14C>G
ENST00000396044.7:c.1885+14C>G	ENSP00000379359.3:n.1885+14C>G
ENST00000504326.5:c.1885+14C>G	ENSP00000421155.1:n.1885+14C>G
ENST00000513847.5:n.2212+14C>G
ENST00000514029.5:c.*366+14C>G	ENSP00000425199.1:n.*366+14C>G
ENST00000612010.4:c.*237+14C>G	ENSP00000482407.1:n.*237+14C>G
ENST00000612452.4:c.1315+14C>G	ENSP00000484033.1:n.1315+14C>G
ENST00000613054.2:c.*83+14C>G	ENSP00000479013.1:n.*83+14C>G
NM_000044.3:c.1885+14C>G	NP_000035.2:n.1885+14C>G
NM_001011645.2:c.289+14C>G	NP_001011645.1:n.289+14C>G
NM_000044.4:c.1885+14C>G	NP_000035.2:n.1885+14C>G
NM_001011645.3:c.289+14C>G	NP_001011645.1:n.289+14C>G
NM_001348061.1:c.1885+14C>G	NP_001334990.1:n.1885+14C>G
NM_001348063.1:c.1885+14C>G	NP_001334992.1:n.1885+14C>G
NM_001348064.1:c.*83+14C>G	NP_001334993.1:n.*83+14C>G
NM_000044.6:c.1885+14C>G MANE Select	NP_000035.2:n.1885+14C>G