Canonical Allele Identifier: CA413423099

Gene: AR

Linked Data

• dbSNP Id: rs2147524354
• gnomAD v4: X-67711471-C-T
• MyVariant Identifiers: chrX:g.66931313C>T (hg19) ; chrX:g.67711471C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711471C>T , CM000685.2:g.67711471C>T	GRCh38
NC_000023.10:g.66931313C>T , CM000685.1:g.66931313C>T	GRCh37
NC_000023.9:g.66848038C>T	NCBI36
NG_009014.2:g.172440C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*303C>T	ENSP00000379358.4:n.*303C>T
ENST00000374690.9:c.1955C>T MANE Select	ENSP00000363822.3:p.Pro652Leu
ENST00000396043.3:c.582C>T	ENSP00000379358.3:n.582C>T
ENST00000396044.8:c.1955C>T	ENSP00000379359.3:p.Pro652Leu
ENST00000612452.5:c.1955C>T	ENSP00000484033.2:p.Pro652Leu
ENST00000374690.7:c.1955C>T	ENSP00000363822.3:p.Pro652Leu
ENST00000396043.2:c.359C>T	ENSP00000379358.2:p.Pro120Leu
ENST00000396044.7:c.1955C>T	ENSP00000379359.3:p.Pro652Leu
ENST00000612452.4:c.1385C>T	ENSP00000484033.1:p.Pro462Leu
NM_000044.3:c.1955C>T	NP_000035.2:p.Pro652Leu
NM_001011645.2:c.359C>T	NP_001011645.1:p.Pro120Leu
NM_000044.4:c.1955C>T	NP_000035.2:p.Pro652Leu
NM_001011645.3:c.359C>T	NP_001011645.1:p.Pro120Leu
NM_000044.6:c.1955C>T MANE Select	NP_000035.2:p.Pro652Leu