Canonical Allele Identifier: CA10436521

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686033A>G , CM000685.2:g.67686033A>G	GRCh38
NC_000023.10:g.66905875A>G , CM000685.1:g.66905875A>G	GRCh37
NC_000023.9:g.66822600A>G	NCBI36
NG_009014.2:g.147002A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.1792A>G MANE Select	NP_000035.2:p.Ser598Gly
ENST00000374690.9:c.1792A>G MANE Select	ENSP00000363822.3:p.Ser598Gly
NM_000044.3:c.1792A>G	NP_000035.2:p.Ser598Gly
NM_000044.4:c.1792A>G	NP_000035.2:p.Ser598Gly
NM_001011645.2:c.196A>G	NP_001011645.1:p.Ser66Gly
NM_001011645.3:c.196A>G	NP_001011645.1:p.Ser66Gly
NM_001348061.1:c.1792A>G	NP_001334990.1:p.Ser598Gly
NM_001348063.1:c.1792A>G	NP_001334992.1:p.Ser598Gly
NM_001348064.1:c.1709A>G	NP_001334993.1:p.Gln570Arg
ENST00000374690.7:c.1792A>G	ENSP00000363822.3:p.Ser598Gly
ENST00000396043.2:c.196A>G	ENSP00000379358.2:p.Ser66Gly
ENST00000396043.3:c.419A>G	ENSP00000379358.3:n.419A>G
ENST00000396043.4:c.*140A>G	ENSP00000379358.4:n.*140A>G
ENST00000396044.7:c.1792A>G	ENSP00000379359.3:p.Ser598Gly
ENST00000396044.8:c.1792A>G	ENSP00000379359.3:p.Ser598Gly
ENST00000504326.5:c.1792A>G	ENSP00000421155.1:p.Ser598Gly
ENST00000513847.5:n.2119A>G
ENST00000514029.5:c.*273A>G	ENSP00000425199.1:n.*273A>G
ENST00000612010.4:c.*144A>G	ENSP00000482407.1:n.*144A>G
ENST00000612452.4:c.1222A>G	ENSP00000484033.1:p.Ser408Gly
ENST00000612452.5:c.1792A>G	ENSP00000484033.2:p.Ser598Gly
ENST00000613054.2:c.1709A>G	ENSP00000479013.1:p.Gln570Arg