Canonical Allele Identifier: CA413423345

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711586C>G , CM000685.2:g.67711586C>G	GRCh38
NC_000023.10:g.66931428C>G , CM000685.1:g.66931428C>G	GRCh37
NC_000023.9:g.66848153C>G	NCBI36
NG_009014.2:g.172555C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2070C>G MANE Select	NP_000035.2:p.His690Gln
ENST00000374690.9:c.2070C>G MANE Select	ENSP00000363822.3:p.His690Gln
NM_000044.3:c.2070C>G	NP_000035.2:p.His690Gln
NM_000044.4:c.2070C>G	NP_000035.2:p.His690Gln
NM_001011645.2:c.474C>G	NP_001011645.1:p.His158Gln
NM_001011645.3:c.474C>G	NP_001011645.1:p.His158Gln
ENST00000374690.7:c.2070C>G	ENSP00000363822.3:p.His690Gln
ENST00000396043.2:c.474C>G	ENSP00000379358.2:p.His158Gln
ENST00000396043.3:c.697C>G	ENSP00000379358.3:n.697C>G
ENST00000396043.4:c.*418C>G	ENSP00000379358.4:n.*418C>G
ENST00000396044.7:c.2070C>G	ENSP00000379359.3:p.His690Gln
ENST00000396044.8:c.2070C>G	ENSP00000379359.3:p.His690Gln
ENST00000612452.4:c.1500C>G	ENSP00000484033.1:p.His500Gln
ENST00000612452.5:c.2070C>G	ENSP00000484033.2:p.His690Gln