Canonical Allele Identifier: CA2435101981
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643400C= , CM000685.2:g.67643400C= GRCh38
NC_000023.10:g.66863242C= , CM000685.1:g.66863242C= GRCh37
NC_000023.9:g.66779967C= NCBI36
NG_009014.2:g.104369C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*109C= ENSP00000379358.4:n.*109C=
ENST00000374690.9:c.1761C= MANE Select ENSP00000363822.3:p.Ala587=
ENST00000396043.3:c.388C= ENSP00000379358.3:n.388C=
ENST00000396044.8:c.1761C= ENSP00000379359.3:p.Ala587=
ENST00000612452.5:c.1761C= ENSP00000484033.2:p.Ala587=
ENST00000374690.7:c.1761C= ENSP00000363822.3:p.Ala587=
ENST00000396043.2:c.165C= ENSP00000379358.2:p.Ala55=
ENST00000396044.7:c.1761C= ENSP00000379359.3:p.Ala587=
ENST00000504326.5:c.1761C= ENSP00000421155.1:p.Ala587=
ENST00000513847.5:n.2088C=
ENST00000514029.5:c.1761C= ENSP00000425199.1:p.Ala587=
ENST00000612010.4:c.1761C= ENSP00000482407.1:p.Ala587=
ENST00000612452.4:c.1191C= ENSP00000484033.1:p.Ala397=
ENST00000613054.2:c.1617-42541C= ENSP00000479013.1:n.1617-42541C=
NM_000044.3:c.1761C= NP_000035.2:p.Ala587=
NM_001011645.2:c.165C= NP_001011645.1:p.Ala55=
NM_000044.4:c.1761C= NP_000035.2:p.Ala587=
NM_001011645.3:c.165C= NP_001011645.1:p.Ala55=
NM_001348061.1:c.1761C= NP_001334990.1:p.Ala587=
NM_001348063.1:c.1761C= NP_001334992.1:p.Ala587=
NM_001348064.1:c.1617-42541C= NP_001334993.1:n.1617-42541C=
NM_000044.6:c.1761C= MANE Select NP_000035.2:p.Ala587=