Canonical Allele Identifier: CA2695234369

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717478_67717479delinsAT , CM000685.2:g.67717478_67717479delinsAT	GRCh38
NC_000023.10:g.66937320_66937321delinsAT , CM000685.1:g.66937320_66937321delinsAT	GRCh37
NC_000023.9:g.66854045_66854046delinsAT	NCBI36
NG_009014.2:g.178447_178448delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522_*523delinsAT	ENSP00000379358.4:n.*522_*523delinsAT
ENST00000374690.9:c.2174_2175delinsAT MANE Select	ENSP00000363822.3:p.Gly725Asp
ENST00000396043.3:c.801_802delinsAT	ENSP00000379358.3:n.801_802delinsAT
ENST00000396044.8:c.2173+5789_2173+5790delinsAT	ENSP00000379359.3:n.2173+5789_2173+5790delinsAT
ENST00000612452.5:c.2174_2175delinsAT	ENSP00000484033.2:p.Gly725Asp
ENST00000374690.7:c.2174_2175delinsAT	ENSP00000363822.3:p.Gly725Asp
ENST00000396043.2:c.578_579delinsAT	ENSP00000379358.2:p.Gly193Asp
ENST00000396044.7:c.2173+5789_2173+5790delinsAT	ENSP00000379359.3:n.2173+5789_2173+5790delinsAT
ENST00000612452.4:c.1604_1605delinsAT	ENSP00000484033.1:p.Gly535Asp
NM_000044.3:c.2174_2175delinsAT	NP_000035.2:p.Gly725Asp
NM_001011645.2:c.578_579delinsAT	NP_001011645.1:p.Gly193Asp
NM_000044.4:c.2174_2175delinsAT	NP_000035.2:p.Gly725Asp
NM_001011645.3:c.578_579delinsAT	NP_001011645.1:p.Gly193Asp
NM_000044.6:c.2174_2175delinsAT MANE Select	NP_000035.2:p.Gly725Asp