Canonical Allele Identifier: CA413423135

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711488C>T , CM000685.2:g.67711488C>T	GRCh38
NC_000023.10:g.66931330C>T , CM000685.1:g.66931330C>T	GRCh37
NC_000023.9:g.66848055C>T	NCBI36
NG_009014.2:g.172457C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.1972C>T MANE Select	NP_000035.2:p.Gln658Ter
ENST00000374690.9:c.1972C>T MANE Select	ENSP00000363822.3:p.Gln658Ter
NM_000044.3:c.1972C>T	NP_000035.2:p.Gln658Ter
NM_000044.4:c.1972C>T	NP_000035.2:p.Gln658Ter
NM_001011645.2:c.376C>T	NP_001011645.1:p.Gln126Ter
NM_001011645.3:c.376C>T	NP_001011645.1:p.Gln126Ter
ENST00000374690.7:c.1972C>T	ENSP00000363822.3:p.Gln658Ter
ENST00000396043.2:c.376C>T	ENSP00000379358.2:p.Gln126Ter
ENST00000396043.3:c.599C>T	ENSP00000379358.3:n.599C>T
ENST00000396043.4:c.*320C>T	ENSP00000379358.4:n.*320C>T
ENST00000396044.7:c.1972C>T	ENSP00000379359.3:p.Gln658Ter
ENST00000396044.8:c.1972C>T	ENSP00000379359.3:p.Gln658Ter
ENST00000612452.4:c.1402C>T	ENSP00000484033.1:p.Gln468Ter
ENST00000612452.5:c.1972C>T	ENSP00000484033.2:p.Gln658Ter