Canonical Allele Identifier: CA413428251

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66943574C>A (hg19) ; chrX:g.67723732C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723732C>A , CM000685.2:g.67723732C>A	GRCh38
NC_000023.10:g.66943574C>A , CM000685.1:g.66943574C>A	GRCh37
NC_000023.9:g.66860299C>A	NCBI36
NG_009014.2:g.184701C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1002C>A	ENSP00000379358.4:n.*1002C>A
ENST00000374690.9:c.2654C>A MANE Select	ENSP00000363822.3:p.Ser885Ter
ENST00000396043.3:c.1281C>A	ENSP00000379358.3:n.1281C>A
ENST00000396044.8:c.*15C>A	ENSP00000379359.3:n.*15C>A
ENST00000612452.5:c.2654C>A	ENSP00000484033.2:p.Ser885Ter
ENST00000374690.7:c.2654C>A	ENSP00000363822.3:p.Ser885Ter
ENST00000396043.2:c.1058C>A	ENSP00000379358.2:p.Ser353Ter
ENST00000396044.7:c.*15C>A	ENSP00000379359.3:n.*15C>A
ENST00000612452.4:c.2105C>A	ENSP00000484033.1:p.Ser702Ter
NM_000044.3:c.2654C>A	NP_000035.2:p.Ser885Ter
NM_001011645.2:c.1058C>A	NP_001011645.1:p.Ser353Ter
NM_000044.4:c.2654C>A	NP_000035.2:p.Ser885Ter
NM_001011645.3:c.1058C>A	NP_001011645.1:p.Ser353Ter
NM_000044.6:c.2654C>A MANE Select	NP_000035.2:p.Ser885Ter