Canonical Allele Identifier: CA2740092167
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2952522
ClinVar RCV Id: RCV003815673

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545490_67545491insCAGATGAGGAACAGCA , CM000685.2:g.67545490_67545491insCAGATGAGGAACAGCA GRCh38
NC_000023.10:g.66765332_66765333insCAGATGAGGAACAGCA , CM000685.1:g.66765332_66765333insCAGATGAGGAACAGCA GRCh37
NC_000023.9:g.66682057_66682058insCAGATGAGGAACAGCA NCBI36
NG_009014.2:g.6459_6460insCAGATGAGGAACAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.344_345insCAGATGAGGAACAGCA ENSP00000379358.4:p.Gln115HisfsTer3
ENST00000374690.9:c.344_345insCAGATGAGGAACAGCA MANE Select ENSP00000363822.3:p.Gln115HisfsTer3
ENST00000396044.8:c.344_345insCAGATGAGGAACAGCA ENSP00000379359.3:p.Gln115HisfsTer3
ENST00000612452.5:c.344_345insCAGATGAGGAACAGCA ENSP00000484033.2:p.Gln115HisfsTer3
ENST00000374690.7:c.344_345insCAGATGAGGAACAGCA ENSP00000363822.3:p.Gln115HisfsTer3
ENST00000396044.7:c.344_345insCAGATGAGGAACAGCA ENSP00000379359.3:p.Gln115HisfsTer3
ENST00000504326.5:c.344_345insCAGATGAGGAACAGCA ENSP00000421155.1:p.Gln115HisfsTer3
ENST00000513847.5:n.671_672insCAGATGAGGAACAGCA
ENST00000514029.5:c.344_345insCAGATGAGGAACAGCA ENSP00000425199.1:p.Gln115HisfsTer3
ENST00000612010.4:c.344_345insCAGATGAGGAACAGCA ENSP00000482407.1:p.Gln115HisfsTer3
ENST00000612452.4:c.-227_-226insCAGATGAGGAACAGCA ENSP00000484033.1:n.-227_-226insCAGATGAGGAACAGCA
ENST00000613054.2:c.344_345insCAGATGAGGAACAGCA ENSP00000479013.1:p.Gln115HisfsTer3
NM_000044.3:c.344_345insCAGATGAGGAACAGCA NP_000035.2:p.Gln115HisfsTer3
NM_000044.4:c.344_345insCAGATGAGGAACAGCA NP_000035.2:p.Gln115HisfsTer3
NM_001011645.3:c.-1440_-1439insCAGATGAGGAACAGCA NP_001011645.1:n.-1440_-1439insCAGATGAGGAACAGCA
NM_001348061.1:c.344_345insCAGATGAGGAACAGCA NP_001334990.1:p.Gln115HisfsTer3
NM_001348063.1:c.344_345insCAGATGAGGAACAGCA NP_001334992.1:p.Gln115HisfsTer3
NM_001348064.1:c.344_345insCAGATGAGGAACAGCA NP_001334993.1:p.Gln115HisfsTer3
NM_000044.6:c.344_345insCAGATGAGGAACAGCA MANE Select NP_000035.2:p.Gln115HisfsTer3