Canonical Allele Identifier: CA413427727

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942717T>A (hg19) ; chrX:g.67722875T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722875T>A , CM000685.2:g.67722875T>A	GRCh38
NC_000023.10:g.66942717T>A , CM000685.1:g.66942717T>A	GRCh37
NC_000023.9:g.66859442T>A	NCBI36
NG_009014.2:g.183844T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*846T>A	ENSP00000379358.4:n.*846T>A
ENST00000374690.9:c.2498T>A MANE Select	ENSP00000363822.3:p.Met833Lys
ENST00000396043.3:c.1125T>A	ENSP00000379358.3:n.1125T>A
ENST00000396044.8:c.2174-811T>A	ENSP00000379359.3:n.2174-811T>A
ENST00000612452.5:c.2498T>A	ENSP00000484033.2:p.Met833Lys
ENST00000374690.7:c.2498T>A	ENSP00000363822.3:p.Met833Lys
ENST00000396043.2:c.902T>A	ENSP00000379358.2:p.Met301Lys
ENST00000396044.7:c.2174-811T>A	ENSP00000379359.3:n.2174-811T>A
ENST00000612452.4:c.1949T>A	ENSP00000484033.1:p.Met650Lys
NM_000044.3:c.2498T>A	NP_000035.2:p.Met833Lys
NM_001011645.2:c.902T>A	NP_001011645.1:p.Met301Lys
NM_000044.4:c.2498T>A	NP_000035.2:p.Met833Lys
NM_001011645.3:c.902T>A	NP_001011645.1:p.Met301Lys
NM_000044.6:c.2498T>A MANE Select	NP_000035.2:p.Met833Lys