Canonical Allele Identifier: CA2435134266

Gene: AR

Linked Data

• dbSNP Id: rs2076136460

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721684_67721687del , CM000685.2:g.67721684_67721687del	GRCh38
NC_000023.10:g.66941526_66941529del , CM000685.1:g.66941526_66941529del	GRCh37
NC_000023.9:g.66858251_66858254del	NCBI36
NG_009014.2:g.182653_182656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667-149_*667-146del	ENSP00000379358.4:n.*667-149_*667-146del
ENST00000374690.9:c.2319-149_2319-146del MANE Select	ENSP00000363822.3:n.2319-149_2319-146del
ENST00000396043.3:c.946-149_946-146del	ENSP00000379358.3:n.946-149_946-146del
ENST00000396044.8:c.2174-2002_2174-1999del	ENSP00000379359.3:n.2174-2002_2174-1999del
ENST00000612452.5:c.2319-149_2319-146del	ENSP00000484033.2:n.2319-149_2319-146del
ENST00000374690.7:c.2319-149_2319-146del	ENSP00000363822.3:n.2319-149_2319-146del
ENST00000396043.2:c.723-149_723-146del	ENSP00000379358.2:n.723-149_723-146del
ENST00000396044.7:c.2174-2002_2174-1999del	ENSP00000379359.3:n.2174-2002_2174-1999del
ENST00000612452.4:c.1749-149_1749-146del	ENSP00000484033.1:n.1749-149_1749-146del
NM_000044.3:c.2319-149_2319-146del	NP_000035.2:n.2319-149_2319-146del
NM_001011645.2:c.723-149_723-146del	NP_001011645.1:n.723-149_723-146del
NM_000044.4:c.2319-149_2319-146del	NP_000035.2:n.2319-149_2319-146del
NM_001011645.3:c.723-149_723-146del	NP_001011645.1:n.723-149_723-146del
NM_000044.6:c.2319-149_2319-146del MANE Select	NP_000035.2:n.2319-149_2319-146del