Canonical Allele Identifier: CA1133902106
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs1929653056

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545336_67545337insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC , CM000685.2:g.67545336_67545337insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC GRCh38
NC_000023.10:g.66765178_66765179insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC , CM000685.1:g.66765178_66765179insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC GRCh37
NC_000023.9:g.66681903_66681904insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NCBI36
NG_009014.2:g.6305_6306insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000379358.4:p.Gln63_Gln64insLeuGlnG...
ENST00000374690.9:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC MANE Select ENSP00000363822.3:p.Gln63_Gln64insLeuGlnG...
ENST00000396044.8:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000379359.3:p.Gln63_Gln64insLeuGlnG...
ENST00000612452.5:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000484033.2:p.Gln63_Gln64insLeuGlnG...
ENST00000374690.7:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000363822.3:p.Gln63_Gln64insLeuGlnG...
ENST00000396044.7:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000379359.3:p.Gln63_Gln64insLeuGlnG...
ENST00000504326.5:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000421155.1:p.Gln63_Gln64insLeuGlnG...
ENST00000513847.5:n.517_518insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC
ENST00000514029.5:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000425199.1:p.Gln63_Gln64insLeuGlnG...
ENST00000612010.4:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000482407.1:p.Gln63_Gln64insLeuGlnG...
ENST00000612452.4:c.-381_-380insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000484033.1:n.-381_-380insTGCAGCAGC...
ENST00000613054.2:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ENSP00000479013.1:p.Gln63_Gln64insLeuGlnG...
NM_000044.3:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_000035.2:p.Gln63_Gln64insLeuGlnGlnGlnG...
NM_000044.4:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_000035.2:p.Gln63_Gln64insLeuGlnGlnGlnG...
NM_001011645.3:c.-1594_-1593insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_001011645.1:n.-1594_-1593insTGCAGCAGCA...
NM_001348061.1:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_001334990.1:p.Gln63_Gln64insLeuGlnGlnG...
NM_001348063.1:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_001334992.1:p.Gln63_Gln64insLeuGlnGlnG...
NM_001348064.1:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC NP_001334993.1:p.Gln63_Gln64insLeuGlnGlnG...
NM_000044.6:c.190_191insTGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC MANE Select NP_000035.2:p.Gln63_Gln64insLeuGlnGlnGlnG...