Canonical Allele Identifier: CA2821593174
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67546233_67546234insTGC , CM000685.2:g.67546233_67546234insTGC GRCh38
NC_000023.10:g.66766075_66766076insTGC , CM000685.1:g.66766075_66766076insTGC GRCh37
NC_000023.9:g.66682800_66682801insTGC NCBI36
NG_009014.2:g.7202_7203insTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.1087_1088insTGC ENSP00000379358.4:p.Asp363delinsValHis
ENST00000374690.9:c.1087_1088insTGC MANE Select ENSP00000363822.3:p.Asp363delinsValHis
ENST00000396044.8:c.1087_1088insTGC ENSP00000379359.3:p.Asp363delinsValHis
ENST00000612452.5:c.1087_1088insTGC ENSP00000484033.2:p.Asp363delinsValHis
ENST00000374690.7:c.1087_1088insTGC ENSP00000363822.3:p.Asp363delinsValHis
ENST00000396044.7:c.1087_1088insTGC ENSP00000379359.3:p.Asp363delinsValHis
ENST00000504326.5:c.1087_1088insTGC ENSP00000421155.1:p.Asp363delinsValHis
ENST00000513847.5:n.1414_1415insTGC
ENST00000514029.5:c.1087_1088insTGC ENSP00000425199.1:p.Asp363delinsValHis
ENST00000612010.4:c.1087_1088insTGC ENSP00000482407.1:p.Asp363delinsValHis
ENST00000612452.4:c.517_518insTGC ENSP00000484033.1:p.Asp173delinsValHis
ENST00000613054.2:c.1087_1088insTGC ENSP00000479013.1:p.Asp363delinsValHis
NM_000044.3:c.1087_1088insTGC NP_000035.2:p.Asp363delinsValHis
NM_000044.4:c.1087_1088insTGC NP_000035.2:p.Asp363delinsValHis
NM_001011645.3:c.-697_-696insTGC NP_001011645.1:n.-697_-696insTGC
NM_001348061.1:c.1087_1088insTGC NP_001334990.1:p.Asp363delinsValHis
NM_001348063.1:c.1087_1088insTGC NP_001334992.1:p.Asp363delinsValHis
NM_001348064.1:c.1087_1088insTGC NP_001334993.1:p.Asp363delinsValHis
NM_000044.6:c.1087_1088insTGC MANE Select NP_000035.2:p.Asp363delinsValHis