Canonical Allele Identifier: CA877547722

Gene: AR

Linked Data

• dbSNP Id: rs966310966
• gnomAD v3: X-67544849-GT-G
• gnomAD v4: X-67544849-GT-G
• MyVariant Identifiers: chrX:g.66764692del (hg19) ; chrX:g.67544850del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67544856del , CM000685.2:g.67544856del	GRCh38
NC_000023.10:g.66764698del , CM000685.1:g.66764698del	GRCh37
NC_000023.9:g.66681423del	NCBI36
NG_009014.2:g.5825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-291del	ENSP00000379358.4:n.-291del
ENST00000374690.9:c.-291del MANE Select	ENSP00000363822.3:n.-291del
ENST00000612452.5:c.-291del	ENSP00000484033.2:n.-291del
ENST00000374690.7:c.-291del	ENSP00000363822.3:n.-291del
ENST00000396044.7:c.-291del	ENSP00000379359.3:n.-291del
ENST00000504326.5:c.-291del	ENSP00000421155.1:n.-291del
ENST00000513847.5:n.37del
ENST00000514029.5:c.-291del	ENSP00000425199.1:n.-291del
ENST00000612010.4:c.-291del	ENSP00000482407.1:n.-291del
ENST00000612452.4:c.-861del	ENSP00000484033.1:n.-861del
ENST00000613054.2:c.-291del	ENSP00000479013.1:n.-291del
NM_000044.3:c.-291del	NP_000035.2:n.-291del
NM_000044.4:c.-291del	NP_000035.2:n.-291del
NM_001011645.3:c.-2074del	NP_001011645.1:n.-2074del
NM_001348061.1:c.-291del	NP_001334990.1:n.-291del
NM_001348063.1:c.-291del	NP_001334992.1:n.-291del
NM_001348064.1:c.-291del	NP_001334993.1:n.-291del
NM_000044.6:c.-291del MANE Select	NP_000035.2:n.-291del