Canonical Allele Identifier: CA2435132618

Gene: AR

Linked Data

• dbSNP Id: rs2076118171

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717464_67717467del , CM000685.2:g.67717464_67717467del	GRCh38
NC_000023.10:g.66937306_66937309del , CM000685.1:g.66937306_66937309del	GRCh37
NC_000023.9:g.66854031_66854034del	NCBI36
NG_009014.2:g.178433_178436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522-14_*522-11del	ENSP00000379358.4:n.*522-14_*522-11del
ENST00000374690.9:c.2174-14_2174-11del MANE Select	ENSP00000363822.3:n.2174-14_2174-11del
ENST00000396043.3:c.801-14_801-11del	ENSP00000379358.3:n.801-14_801-11del
ENST00000396044.8:c.2173+5775_2173+5778del	ENSP00000379359.3:n.2173+5775_2173+5778del
ENST00000612452.5:c.2174-14_2174-11del	ENSP00000484033.2:n.2174-14_2174-11del
ENST00000374690.7:c.2174-14_2174-11del	ENSP00000363822.3:n.2174-14_2174-11del
ENST00000396043.2:c.578-14_578-11del	ENSP00000379358.2:n.578-14_578-11del
ENST00000396044.7:c.2173+5775_2173+5778del	ENSP00000379359.3:n.2173+5775_2173+5778del
ENST00000612452.4:c.1604-14_1604-11del	ENSP00000484033.1:n.1604-14_1604-11del
NM_000044.3:c.2174-14_2174-11del	NP_000035.2:n.2174-14_2174-11del
NM_001011645.2:c.578-14_578-11del	NP_001011645.1:n.578-14_578-11del
NM_000044.4:c.2174-14_2174-11del	NP_000035.2:n.2174-14_2174-11del
NM_001011645.3:c.578-14_578-11del	NP_001011645.1:n.578-14_578-11del
NM_000044.6:c.2174-14_2174-11del MANE Select	NP_000035.2:n.2174-14_2174-11del