Canonical Allele Identifier: CA516970416

Gene: AR

Linked Data

• dbSNP Id: rs2147531118
• MyVariant Identifiers: chrX:g.66937444C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717602C>A , CM000685.2:g.67717602C>A	GRCh38
NC_000023.10:g.66937444C>A , CM000685.1:g.66937444C>A	GRCh37
NC_000023.9:g.66854169C>A	NCBI36
NG_009014.2:g.178571C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*646C>A	ENSP00000379358.4:n.*646C>A
ENST00000374690.9:c.2298C>A MANE Select	ENSP00000363822.3:p.Ala766=
ENST00000396043.3:c.925C>A	ENSP00000379358.3:n.925C>A
ENST00000396044.8:c.2173+5913C>A	ENSP00000379359.3:n.2173+5913C>A
ENST00000612452.5:c.2298C>A	ENSP00000484033.2:p.Ala766=
ENST00000374690.7:c.2298C>A	ENSP00000363822.3:p.Ala766=
ENST00000396043.2:c.702C>A	ENSP00000379358.2:p.Ala234=
ENST00000396044.7:c.2173+5913C>A	ENSP00000379359.3:n.2173+5913C>A
ENST00000612452.4:c.1728C>A	ENSP00000484033.1:p.Ala576=
NM_000044.3:c.2298C>A	NP_000035.2:p.Ala766=
NM_001011645.2:c.702C>A	NP_001011645.1:p.Ala234=
NM_000044.4:c.2298C>A	NP_000035.2:p.Ala766=
NM_001011645.3:c.702C>A	NP_001011645.1:p.Ala234=
NM_000044.6:c.2298C>A MANE Select	NP_000035.2:p.Ala766=