Canonical Allele Identifier: CA1133901956
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs755686403

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545315_67545316insAGCAGCAGCAGCAGC , CM000685.2:g.67545315_67545316insAGCAGCAGCAGCAGC GRCh38
NC_000023.10:g.66765157_66765158insAGCAGCAGCAGCAGC , CM000685.1:g.66765157_66765158insAGCAGCAGCAGCAGC GRCh37
NC_000023.9:g.66681882_66681883insAGCAGCAGCAGCAGC NCBI36
NG_009014.2:g.6284_6285insAGCAGCAGCAGCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.169_170insAGCAGCAGCAGCAGC ENSP00000379358.4:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000374690.9:c.169_170insAGCAGCAGCAGCAGC MANE Select ENSP00000363822.3:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000396044.8:c.169_170insAGCAGCAGCAGCAGC ENSP00000379359.3:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000612452.5:c.169_170insAGCAGCAGCAGCAGC ENSP00000484033.2:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000374690.7:c.169_170insAGCAGCAGCAGCAGC ENSP00000363822.3:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000396044.7:c.169_170insAGCAGCAGCAGCAGC ENSP00000379359.3:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000504326.5:c.169_170insAGCAGCAGCAGCAGC ENSP00000421155.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000513847.5:n.496_497insAGCAGCAGCAGCAGC
ENST00000514029.5:c.169_170insAGCAGCAGCAGCAGC ENSP00000425199.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000612010.4:c.169_170insAGCAGCAGCAGCAGC ENSP00000482407.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
ENST00000612452.4:c.-402_-401insAGCAGCAGCAGCAGC ENSP00000484033.1:n.-402_-401insAGCAGCAGCAGCAGC
ENST00000613054.2:c.169_170insAGCAGCAGCAGCAGC ENSP00000479013.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_000044.3:c.169_170insAGCAGCAGCAGCAGC NP_000035.2:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_000044.4:c.169_170insAGCAGCAGCAGCAGC NP_000035.2:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_001011645.3:c.-1615_-1614insAGCAGCAGCAGCAGC NP_001011645.1:n.-1615_-1614insAGCAGCAGCAGCAGC
NM_001348061.1:c.169_170insAGCAGCAGCAGCAGC NP_001334990.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_001348063.1:c.169_170insAGCAGCAGCAGCAGC NP_001334992.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_001348064.1:c.169_170insAGCAGCAGCAGCAGC NP_001334993.1:p.Leu56_Leu57insGlnGlnGlnGlnGln
NM_000044.6:c.169_170insAGCAGCAGCAGCAGC MANE Select NP_000035.2:p.Leu56_Leu57insGlnGlnGlnGlnGln