Canonical Allele Identifier: CA2435119870

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686074T= , CM000685.2:g.67686074T=	GRCh38
NC_000023.10:g.66905916T= , CM000685.1:g.66905916T=	GRCh37
NC_000023.9:g.66822641T=	NCBI36
NG_009014.2:g.147043T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*181T=	ENSP00000379358.4:n.*181T=
ENST00000374690.9:c.1833T= MANE Select	ENSP00000363822.3:p.Asn611=
ENST00000396043.3:c.460T=	ENSP00000379358.3:n.460T=
ENST00000396044.8:c.1833T=	ENSP00000379359.3:p.Asn611=
ENST00000612452.5:c.1833T=	ENSP00000484033.2:p.Asn611=
ENST00000374690.7:c.1833T=	ENSP00000363822.3:p.Asn611=
ENST00000396043.2:c.237T=	ENSP00000379358.2:p.Asn79=
ENST00000396044.7:c.1833T=	ENSP00000379359.3:p.Asn611=
ENST00000504326.5:c.1833T=	ENSP00000421155.1:p.Asn611=
ENST00000513847.5:n.2160T=
ENST00000514029.5:c.*314T=	ENSP00000425199.1:n.*314T=
ENST00000612010.4:c.*185T=	ENSP00000482407.1:n.*185T=
ENST00000612452.4:c.1263T=	ENSP00000484033.1:p.Asn421=
ENST00000613054.2:c.*31T=	ENSP00000479013.1:n.*31T=
NM_000044.3:c.1833T=	NP_000035.2:p.Asn611=
NM_001011645.2:c.237T=	NP_001011645.1:p.Asn79=
NM_000044.4:c.1833T=	NP_000035.2:p.Asn611=
NM_001011645.3:c.237T=	NP_001011645.1:p.Asn79=
NM_001348061.1:c.1833T=	NP_001334990.1:p.Asn611=
NM_001348063.1:c.1833T=	NP_001334992.1:p.Asn611=
NM_001348064.1:c.*31T=	NP_001334993.1:n.*31T=
NM_000044.6:c.1833T= MANE Select	NP_000035.2:p.Asn611=