Canonical Allele Identifier: CA330772219

Gene: AR

Linked Data

• dbSNP Id: rs753767208
• gnomAD v2: X-66941497-AAAAC-A
• gnomAD v3: X-67721655-AAAAC-A
• gnomAD v4: X-67721655-AAAAC-A
• MyVariant Identifiers: chrX:g.66941498_66941501del (hg19) ; chrX:g.67721656_67721659del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721665_67721668del , CM000685.2:g.67721665_67721668del	GRCh38
NC_000023.10:g.66941507_66941510del , CM000685.1:g.66941507_66941510del	GRCh37
NC_000023.9:g.66858232_66858235del	NCBI36
NG_009014.2:g.182634_182637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667-168_*667-165del	ENSP00000379358.4:n.*667-168_*667-165del
ENST00000374690.9:c.2319-168_2319-165del MANE Select	ENSP00000363822.3:n.2319-168_2319-165del
ENST00000396043.3:c.946-168_946-165del	ENSP00000379358.3:n.946-168_946-165del
ENST00000396044.8:c.2174-2021_2174-2018del	ENSP00000379359.3:n.2174-2021_2174-2018del
ENST00000612452.5:c.2319-168_2319-165del	ENSP00000484033.2:n.2319-168_2319-165del
ENST00000374690.7:c.2319-168_2319-165del	ENSP00000363822.3:n.2319-168_2319-165del
ENST00000396043.2:c.723-168_723-165del	ENSP00000379358.2:n.723-168_723-165del
ENST00000396044.7:c.2174-2021_2174-2018del	ENSP00000379359.3:n.2174-2021_2174-2018del
ENST00000612452.4:c.1749-168_1749-165del	ENSP00000484033.1:n.1749-168_1749-165del
NM_000044.3:c.2319-168_2319-165del	NP_000035.2:n.2319-168_2319-165del
NM_001011645.2:c.723-168_723-165del	NP_001011645.1:n.723-168_723-165del
NM_000044.4:c.2319-168_2319-165del	NP_000035.2:n.2319-168_2319-165del
NM_001011645.3:c.723-168_723-165del	NP_001011645.1:n.723-168_723-165del
NM_000044.6:c.2319-168_2319-165del MANE Select	NP_000035.2:n.2319-168_2319-165del