Canonical Allele Identifier: CA10436608

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717574A>G , CM000685.2:g.67717574A>G	GRCh38
NC_000023.10:g.66937416A>G , CM000685.1:g.66937416A>G	GRCh37
NC_000023.9:g.66854141A>G	NCBI36
NG_009014.2:g.178543A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2270A>G MANE Select	NP_000035.2:p.Asn757Ser
ENST00000374690.9:c.2270A>G MANE Select	ENSP00000363822.3:p.Asn757Ser
NM_000044.3:c.2270A>G	NP_000035.2:p.Asn757Ser
NM_000044.4:c.2270A>G	NP_000035.2:p.Asn757Ser
NM_001011645.2:c.674A>G	NP_001011645.1:p.Asn225Ser
NM_001011645.3:c.674A>G	NP_001011645.1:p.Asn225Ser
ENST00000374690.7:c.2270A>G	ENSP00000363822.3:p.Asn757Ser
ENST00000396043.2:c.674A>G	ENSP00000379358.2:p.Asn225Ser
ENST00000396043.3:c.897A>G	ENSP00000379358.3:n.897A>G
ENST00000396043.4:c.*618A>G	ENSP00000379358.4:n.*618A>G
ENST00000396044.7:c.2173+5885A>G	ENSP00000379359.3:n.2173+5885A>G
ENST00000396044.8:c.2173+5885A>G	ENSP00000379359.3:n.2173+5885A>G
ENST00000612452.4:c.1700A>G	ENSP00000484033.1:p.Asn567Ser
ENST00000612452.5:c.2270A>G	ENSP00000484033.2:p.Asn757Ser