Canonical Allele Identifier: CA10436696

Gene: AR

Linked Data

• ClinVar Variation Id: 1635104
• ClinVar RCV Id: RCV002133204
• dbSNP Id: rs749355366
• ExAC: X:66943508 CCT / C
• gnomAD v2: X-66943508-CCT-C
• gnomAD v3: X-67723666-CCT-C
• gnomAD v4: X-67723666-CCT-C
• MyVariant Identifiers: chrX:g.66943509_66943510del (hg19) ; chrX:g.67723667_67723668del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723669_67723670del , CM000685.2:g.67723669_67723670del	GRCh38
NC_000023.10:g.66943511_66943512del , CM000685.1:g.66943511_66943512del	GRCh37
NC_000023.9:g.66860236_66860237del	NCBI36
NG_009014.2:g.184638_184639del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*956-17_*956-16del	ENSP00000379358.4:n.*956-17_*956-16del
ENST00000374690.9:c.2608-17_2608-16del MANE Select	ENSP00000363822.3:n.2608-17_2608-16del
ENST00000396043.3:c.1235-17_1235-16del	ENSP00000379358.3:n.1235-17_1235-16del
ENST00000396044.8:c.2174-17_2174-16del	ENSP00000379359.3:n.2174-17_2174-16del
ENST00000612452.5:c.2608-17_2608-16del	ENSP00000484033.2:n.2608-17_2608-16del
ENST00000374690.7:c.2608-17_2608-16del	ENSP00000363822.3:n.2608-17_2608-16del
ENST00000396043.2:c.1012-17_1012-16del	ENSP00000379358.2:n.1012-17_1012-16del
ENST00000396044.7:c.2174-17_2174-16del	ENSP00000379359.3:n.2174-17_2174-16del
ENST00000612452.4:c.2059-17_2059-16del	ENSP00000484033.1:n.2059-17_2059-16del
NM_000044.3:c.2608-17_2608-16del	NP_000035.2:n.2608-17_2608-16del
NM_001011645.2:c.1012-17_1012-16del	NP_001011645.1:n.1012-17_1012-16del
NM_000044.4:c.2608-17_2608-16del	NP_000035.2:n.2608-17_2608-16del
NM_001011645.3:c.1012-17_1012-16del	NP_001011645.1:n.1012-17_1012-16del
NM_000044.6:c.2608-17_2608-16del MANE Select	NP_000035.2:n.2608-17_2608-16del