Canonical Allele Identifier: CA413422908

Gene: AR

Linked Data

• ClinVar Variation Id: 2077770
• ClinVar RCV Id: RCV002985696
• dbSNP Id: rs767711979
• MyVariant Identifiers: chrX:g.66863237A>T (hg19) ; chrX:g.67643395A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643395A>T , CM000685.2:g.67643395A>T	GRCh38
NC_000023.10:g.66863237A>T , CM000685.1:g.66863237A>T	GRCh37
NC_000023.9:g.66779962A>T	NCBI36
NG_009014.2:g.104364A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*104A>T	ENSP00000379358.4:n.*104A>T
ENST00000374690.9:c.1756A>T MANE Select	ENSP00000363822.3:p.Arg586Ter
ENST00000396043.3:c.383A>T	ENSP00000379358.3:n.383A>T
ENST00000396044.8:c.1756A>T	ENSP00000379359.3:p.Arg586Ter
ENST00000612452.5:c.1756A>T	ENSP00000484033.2:p.Arg586Ter
ENST00000374690.7:c.1756A>T	ENSP00000363822.3:p.Arg586Ter
ENST00000396043.2:c.160A>T	ENSP00000379358.2:p.Arg54Ter
ENST00000396044.7:c.1756A>T	ENSP00000379359.3:p.Arg586Ter
ENST00000504326.5:c.1756A>T	ENSP00000421155.1:p.Arg586Ter
ENST00000513847.5:n.2083A>T
ENST00000514029.5:c.1756A>T	ENSP00000425199.1:p.Arg586Ter
ENST00000612010.4:c.1756A>T	ENSP00000482407.1:p.Arg586Ter
ENST00000612452.4:c.1186A>T	ENSP00000484033.1:p.Arg396Ter
ENST00000613054.2:c.1617-42546A>T	ENSP00000479013.1:n.1617-42546A>T
NM_000044.3:c.1756A>T	NP_000035.2:p.Arg586Ter
NM_001011645.2:c.160A>T	NP_001011645.1:p.Arg54Ter
NM_000044.4:c.1756A>T	NP_000035.2:p.Arg586Ter
NM_001011645.3:c.160A>T	NP_001011645.1:p.Arg54Ter
NM_001348061.1:c.1756A>T	NP_001334990.1:p.Arg586Ter
NM_001348063.1:c.1756A>T	NP_001334992.1:p.Arg586Ter
NM_001348064.1:c.1617-42546A>T	NP_001334993.1:n.1617-42546A>T
NM_000044.6:c.1756A>T MANE Select	NP_000035.2:p.Arg586Ter