Canonical Allele Identifier: CA2435101865

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643069_67643071delinsGCT , CM000685.2:g.67643069_67643071delinsGCT	GRCh38
NC_000023.10:g.66862911_66862913delinsGCT , CM000685.1:g.66862911_66862913delinsGCT	GRCh37
NC_000023.9:g.66779636_66779638delinsGCT	NCBI36
NG_009014.2:g.104038_104040delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.1804-187_1804-185delinsGCT	ENSP00000379358.4:n.1804-187_1804-185delinsGCT
ENST00000374690.9:c.1617-187_1617-185delinsGCT MANE Select	ENSP00000363822.3:n.1617-187_1617-185delinsGCT
ENST00000396043.3:c.244-187_244-185delinsGCT	ENSP00000379358.3:n.244-187_244-185delinsGCT
ENST00000396044.8:c.1617-187_1617-185delinsGCT	ENSP00000379359.3:n.1617-187_1617-185delinsGCT
ENST00000612452.5:c.1617-187_1617-185delinsGCT	ENSP00000484033.2:n.1617-187_1617-185delinsGCT
ENST00000374690.7:c.1617-187_1617-185delinsGCT	ENSP00000363822.3:n.1617-187_1617-185delinsGCT
ENST00000396043.2:c.21-187_21-185delinsGCT	ENSP00000379358.2:n.21-187_21-185delinsGCT
ENST00000396044.7:c.1617-187_1617-185delinsGCT	ENSP00000379359.3:n.1617-187_1617-185delinsGCT
ENST00000504326.5:c.1617-187_1617-185delinsGCT	ENSP00000421155.1:n.1617-187_1617-185delinsGCT
ENST00000513847.5:n.1944-187_1944-185delinsGCT
ENST00000514029.5:c.1617-187_1617-185delinsGCT	ENSP00000425199.1:n.1617-187_1617-185delinsGCT
ENST00000612010.4:c.1617-187_1617-185delinsGCT	ENSP00000482407.1:n.1617-187_1617-185delinsGCT
ENST00000612452.4:c.1047-187_1047-185delinsGCT	ENSP00000484033.1:n.1047-187_1047-185delinsGCT
ENST00000613054.2:c.1617-42872_1617-42870delinsGCT	ENSP00000479013.1:n.1617-42872_1617-42870delinsGCT
NM_000044.3:c.1617-187_1617-185delinsGCT	NP_000035.2:n.1617-187_1617-185delinsGCT
NM_001011645.2:c.21-187_21-185delinsGCT	NP_001011645.1:n.21-187_21-185delinsGCT
NM_000044.4:c.1617-187_1617-185delinsGCT	NP_000035.2:n.1617-187_1617-185delinsGCT
NM_001011645.3:c.21-187_21-185delinsGCT	NP_001011645.1:n.21-187_21-185delinsGCT
NM_001348061.1:c.1617-187_1617-185delinsGCT	NP_001334990.1:n.1617-187_1617-185delinsGCT
NM_001348063.1:c.1617-187_1617-185delinsGCT	NP_001334992.1:n.1617-187_1617-185delinsGCT
NM_001348064.1:c.1617-42872_1617-42870delinsGCT	NP_001334993.1:n.1617-42872_1617-42870delinsGCT
NM_000044.6:c.1617-187_1617-185delinsGCT MANE Select	NP_000035.2:n.1617-187_1617-185delinsGCT