Canonical Allele Identifier: CA413424500
Community Standard Title: NM_000044.6(AR):c.2220C>G (p.Tyr740Ter)
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717524C>G , CM000685.2:g.67717524C>G GRCh38
NC_000023.10:g.66937366C>G , CM000685.1:g.66937366C>G GRCh37
NC_000023.9:g.66854091C>G NCBI36
NG_009014.2:g.178493C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2220C>G MANE Select NP_000035.2:p.Tyr740Ter
ENST00000374690.9:c.2220C>G MANE Select ENSP00000363822.3:p.Tyr740Ter
NM_000044.3:c.2220C>G NP_000035.2:p.Tyr740Ter
NM_000044.4:c.2220C>G NP_000035.2:p.Tyr740Ter
NM_001011645.2:c.624C>G NP_001011645.1:p.Tyr208Ter
NM_001011645.3:c.624C>G NP_001011645.1:p.Tyr208Ter
ENST00000374690.7:c.2220C>G ENSP00000363822.3:p.Tyr740Ter
ENST00000396043.2:c.624C>G ENSP00000379358.2:p.Tyr208Ter
ENST00000396043.3:c.847C>G ENSP00000379358.3:n.847C>G
ENST00000396043.4:c.*568C>G ENSP00000379358.4:n.*568C>G
ENST00000396044.7:c.2173+5835C>G ENSP00000379359.3:n.2173+5835C>G
ENST00000396044.8:c.2173+5835C>G ENSP00000379359.3:n.2173+5835C>G
ENST00000612452.4:c.1650C>G ENSP00000484033.1:p.Tyr550Ter
ENST00000612452.5:c.2220C>G ENSP00000484033.2:p.Tyr740Ter