Canonical Allele Identifier: CA2435134700

Gene: AR

Linked Data

• dbSNP Id: rs2076146527
• gnomAD v4: X-67723640-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723644_67723646del , CM000685.2:g.67723644_67723646del	GRCh38
NC_000023.10:g.66943486_66943488del , CM000685.1:g.66943486_66943488del	GRCh37
NC_000023.9:g.66860211_66860213del	NCBI36
NG_009014.2:g.184613_184615del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*956-42_*956-40del	ENSP00000379358.4:n.*956-42_*956-40del
ENST00000374690.9:c.2608-42_2608-40del MANE Select	ENSP00000363822.3:n.2608-42_2608-40del
ENST00000396043.3:c.1235-42_1235-40del	ENSP00000379358.3:n.1235-42_1235-40del
ENST00000396044.8:c.2174-42_2174-40del	ENSP00000379359.3:n.2174-42_2174-40del
ENST00000612452.5:c.2608-42_2608-40del	ENSP00000484033.2:n.2608-42_2608-40del
ENST00000374690.7:c.2608-42_2608-40del	ENSP00000363822.3:n.2608-42_2608-40del
ENST00000396043.2:c.1012-42_1012-40del	ENSP00000379358.2:n.1012-42_1012-40del
ENST00000396044.7:c.2174-42_2174-40del	ENSP00000379359.3:n.2174-42_2174-40del
ENST00000612452.4:c.2059-42_2059-40del	ENSP00000484033.1:n.2059-42_2059-40del
NM_000044.3:c.2608-42_2608-40del	NP_000035.2:n.2608-42_2608-40del
NM_001011645.2:c.1012-42_1012-40del	NP_001011645.1:n.1012-42_1012-40del
NM_000044.4:c.2608-42_2608-40del	NP_000035.2:n.2608-42_2608-40del
NM_001011645.3:c.1012-42_1012-40del	NP_001011645.1:n.1012-42_1012-40del
NM_000044.6:c.2608-42_2608-40del MANE Select	NP_000035.2:n.2608-42_2608-40del