Canonical Allele Identifier: CA2435119840

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67685971_67685974delinsCATT , CM000685.2:g.67685971_67685974delinsCATT	GRCh38
NC_000023.10:g.66905813_66905816delinsCATT , CM000685.1:g.66905813_66905816delinsCATT	GRCh37
NC_000023.9:g.66822538_66822541delinsCATT	NCBI36
NG_009014.2:g.146940_146943delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*117-39_*117-36delinsCATT	ENSP00000379358.4:n.*117-39_*117-36delinsCATT
ENST00000374690.9:c.1769-39_1769-36delinsCATT MANE Select	ENSP00000363822.3:n.1769-39_1769-36delinsCATT
ENST00000396043.3:c.396-39_396-36delinsCATT	ENSP00000379358.3:n.396-39_396-36delinsCATT
ENST00000396044.8:c.1769-39_1769-36delinsCATT	ENSP00000379359.3:n.1769-39_1769-36delinsCATT
ENST00000612452.5:c.1769-39_1769-36delinsCATT	ENSP00000484033.2:n.1769-39_1769-36delinsCATT
ENST00000374690.7:c.1769-39_1769-36delinsCATT	ENSP00000363822.3:n.1769-39_1769-36delinsCATT
ENST00000396043.2:c.173-39_173-36delinsCATT	ENSP00000379358.2:n.173-39_173-36delinsCATT
ENST00000396044.7:c.1769-39_1769-36delinsCATT	ENSP00000379359.3:n.1769-39_1769-36delinsCATT
ENST00000504326.5:c.1769-39_1769-36delinsCATT	ENSP00000421155.1:n.1769-39_1769-36delinsCATT
ENST00000513847.5:n.2096-39_2096-36delinsCATT
ENST00000514029.5:c.*250-39_*250-36delinsCATT	ENSP00000425199.1:n.*250-39_*250-36delinsCATT
ENST00000612010.4:c.*121-39_*121-36delinsCATT	ENSP00000482407.1:n.*121-39_*121-36delinsCATT
ENST00000612452.4:c.1199-39_1199-36delinsCATT	ENSP00000484033.1:n.1199-39_1199-36delinsCATT
ENST00000613054.2:c.1647_1650delinsCATT	ENSP00000479013.1:p.Leu549=
NM_000044.3:c.1769-39_1769-36delinsCATT	NP_000035.2:n.1769-39_1769-36delinsCATT
NM_001011645.2:c.173-39_173-36delinsCATT	NP_001011645.1:n.173-39_173-36delinsCATT
NM_000044.4:c.1769-39_1769-36delinsCATT	NP_000035.2:n.1769-39_1769-36delinsCATT
NM_001011645.3:c.173-39_173-36delinsCATT	NP_001011645.1:n.173-39_173-36delinsCATT
NM_001348061.1:c.1769-39_1769-36delinsCATT	NP_001334990.1:n.1769-39_1769-36delinsCATT
NM_001348063.1:c.1769-39_1769-36delinsCATT	NP_001334992.1:n.1769-39_1769-36delinsCATT
NM_001348064.1:c.1647_1650delinsCATT	NP_001334993.1:p.Leu549=
NM_000044.6:c.1769-39_1769-36delinsCATT MANE Select	NP_000035.2:n.1769-39_1769-36delinsCATT