Canonical Allele Identifier: CA2435134729

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723666_67723668delinsCCT , CM000685.2:g.67723666_67723668delinsCCT	GRCh38
NC_000023.10:g.66943508_66943510delinsCCT , CM000685.1:g.66943508_66943510delinsCCT	GRCh37
NC_000023.9:g.66860233_66860235delinsCCT	NCBI36
NG_009014.2:g.184635_184637delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*956-20_*956-18delinsCCT	ENSP00000379358.4:n.*956-20_*956-18delinsCCT
ENST00000374690.9:c.2608-20_2608-18delinsCCT MANE Select	ENSP00000363822.3:n.2608-20_2608-18delinsCCT
ENST00000396043.3:c.1235-20_1235-18delinsCCT	ENSP00000379358.3:n.1235-20_1235-18delinsCCT
ENST00000396044.8:c.2174-20_2174-18delinsCCT	ENSP00000379359.3:n.2174-20_2174-18delinsCCT
ENST00000612452.5:c.2608-20_2608-18delinsCCT	ENSP00000484033.2:n.2608-20_2608-18delinsCCT
ENST00000374690.7:c.2608-20_2608-18delinsCCT	ENSP00000363822.3:n.2608-20_2608-18delinsCCT
ENST00000396043.2:c.1012-20_1012-18delinsCCT	ENSP00000379358.2:n.1012-20_1012-18delinsCCT
ENST00000396044.7:c.2174-20_2174-18delinsCCT	ENSP00000379359.3:n.2174-20_2174-18delinsCCT
ENST00000612452.4:c.2059-20_2059-18delinsCCT	ENSP00000484033.1:n.2059-20_2059-18delinsCCT
NM_000044.3:c.2608-20_2608-18delinsCCT	NP_000035.2:n.2608-20_2608-18delinsCCT
NM_001011645.2:c.1012-20_1012-18delinsCCT	NP_001011645.1:n.1012-20_1012-18delinsCCT
NM_000044.4:c.2608-20_2608-18delinsCCT	NP_000035.2:n.2608-20_2608-18delinsCCT
NM_001011645.3:c.1012-20_1012-18delinsCCT	NP_001011645.1:n.1012-20_1012-18delinsCCT
NM_000044.6:c.2608-20_2608-18delinsCCT MANE Select	NP_000035.2:n.2608-20_2608-18delinsCCT