Canonical Allele Identifier: CA2435119828

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67685945_67685946delinsAC , CM000685.2:g.67685945_67685946delinsAC	GRCh38
NC_000023.10:g.66905787_66905788delinsAC , CM000685.1:g.66905787_66905788delinsAC	GRCh37
NC_000023.9:g.66822512_66822513delinsAC	NCBI36
NG_009014.2:g.146914_146915delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*117-65_*117-64delinsAC	ENSP00000379358.4:n.*117-65_*117-64delinsAC
ENST00000374690.9:c.1769-65_1769-64delinsAC MANE Select	ENSP00000363822.3:n.1769-65_1769-64delinsAC
ENST00000396043.3:c.396-65_396-64delinsAC	ENSP00000379358.3:n.396-65_396-64delinsAC
ENST00000396044.8:c.1769-65_1769-64delinsAC	ENSP00000379359.3:n.1769-65_1769-64delinsAC
ENST00000612452.5:c.1769-65_1769-64delinsAC	ENSP00000484033.2:n.1769-65_1769-64delinsAC
ENST00000374690.7:c.1769-65_1769-64delinsAC	ENSP00000363822.3:n.1769-65_1769-64delinsAC
ENST00000396043.2:c.173-65_173-64delinsAC	ENSP00000379358.2:n.173-65_173-64delinsAC
ENST00000396044.7:c.1769-65_1769-64delinsAC	ENSP00000379359.3:n.1769-65_1769-64delinsAC
ENST00000504326.5:c.1769-65_1769-64delinsAC	ENSP00000421155.1:n.1769-65_1769-64delinsAC
ENST00000513847.5:n.2096-65_2096-64delinsAC
ENST00000514029.5:c.*250-65_*250-64delinsAC	ENSP00000425199.1:n.*250-65_*250-64delinsAC
ENST00000612010.4:c.*121-65_*121-64delinsAC	ENSP00000482407.1:n.*121-65_*121-64delinsAC
ENST00000612452.4:c.1199-65_1199-64delinsAC	ENSP00000484033.1:n.1199-65_1199-64delinsAC
ENST00000613054.2:c.1621_1622delinsAC	ENSP00000479013.1:p.Thr541=
NM_000044.3:c.1769-65_1769-64delinsAC	NP_000035.2:n.1769-65_1769-64delinsAC
NM_001011645.2:c.173-65_173-64delinsAC	NP_001011645.1:n.173-65_173-64delinsAC
NM_000044.4:c.1769-65_1769-64delinsAC	NP_000035.2:n.1769-65_1769-64delinsAC
NM_001011645.3:c.173-65_173-64delinsAC	NP_001011645.1:n.173-65_173-64delinsAC
NM_001348061.1:c.1769-65_1769-64delinsAC	NP_001334990.1:n.1769-65_1769-64delinsAC
NM_001348063.1:c.1769-65_1769-64delinsAC	NP_001334992.1:n.1769-65_1769-64delinsAC
NM_001348064.1:c.1621_1622delinsAC	NP_001334993.1:p.Thr541=
NM_000044.6:c.1769-65_1769-64delinsAC MANE Select	NP_000035.2:n.1769-65_1769-64delinsAC