Canonical Allele Identifier: CA413424808

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717622A>G , CM000685.2:g.67717622A>G	GRCh38
NC_000023.10:g.66937464A>G , CM000685.1:g.66937464A>G	GRCh37
NC_000023.9:g.66854189A>G	NCBI36
NG_009014.2:g.178591A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2318A>G MANE Select	NP_000035.2:p.Glu773Gly
ENST00000374690.9:c.2318A>G MANE Select	ENSP00000363822.3:p.Glu773Gly
NM_000044.3:c.2318A>G	NP_000035.2:p.Glu773Gly
NM_000044.4:c.2318A>G	NP_000035.2:p.Glu773Gly
NM_001011645.2:c.722A>G	NP_001011645.1:p.Glu241Gly
NM_001011645.3:c.722A>G	NP_001011645.1:p.Glu241Gly
ENST00000374690.7:c.2318A>G	ENSP00000363822.3:p.Glu773Gly
ENST00000396043.2:c.722A>G	ENSP00000379358.2:p.Glu241Gly
ENST00000396043.3:c.945A>G	ENSP00000379358.3:n.945A>G
ENST00000396043.4:c.*666A>G	ENSP00000379358.4:n.*666A>G
ENST00000396044.7:c.2173+5933A>G	ENSP00000379359.3:n.2173+5933A>G
ENST00000396044.8:c.2173+5933A>G	ENSP00000379359.3:n.2173+5933A>G
ENST00000612452.4:c.1748A>G	ENSP00000484033.1:p.Glu583Gly
ENST00000612452.5:c.2318A>G	ENSP00000484033.2:p.Glu773Gly