Canonical Allele Identifier: CA413428121

Gene: AR

Linked Data

• dbSNP Id: rs2147538355
• gnomAD v4: X-67722983-C-T
• MyVariant Identifiers: chrX:g.66942825C>T (hg19) ; chrX:g.67722983C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722983C>T , CM000685.2:g.67722983C>T	GRCh38
NC_000023.10:g.66942825C>T , CM000685.1:g.66942825C>T	GRCh37
NC_000023.9:g.66859550C>T	NCBI36
NG_009014.2:g.183952C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*954C>T	ENSP00000379358.4:n.*954C>T
ENST00000374690.9:c.2606C>T MANE Select	ENSP00000363822.3:p.Pro869Leu
ENST00000396043.3:c.1233C>T	ENSP00000379358.3:n.1233C>T
ENST00000396044.8:c.2174-703C>T	ENSP00000379359.3:n.2174-703C>T
ENST00000612452.5:c.2606C>T	ENSP00000484033.2:p.Pro869Leu
ENST00000374690.7:c.2606C>T	ENSP00000363822.3:p.Pro869Leu
ENST00000396043.2:c.1010C>T	ENSP00000379358.2:p.Pro337Leu
ENST00000396044.7:c.2174-703C>T	ENSP00000379359.3:n.2174-703C>T
ENST00000612452.4:c.2057C>T	ENSP00000484033.1:p.Pro686Leu
NM_000044.3:c.2606C>T	NP_000035.2:p.Pro869Leu
NM_001011645.2:c.1010C>T	NP_001011645.1:p.Pro337Leu
NM_000044.4:c.2606C>T	NP_000035.2:p.Pro869Leu
NM_001011645.3:c.1010C>T	NP_001011645.1:p.Pro337Leu
NM_000044.6:c.2606C>T MANE Select	NP_000035.2:p.Pro869Leu