Canonical Allele Identifier: CA10436236

Gene: AR

Linked Data

• ClinVar Variation Id: 402390
• ClinVar RCV Id: RCV000455544 ; RCV000766100 ; RCV003983052
• dbSNP Id: rs200185441
• ExAC: X:66765161 A / T
• gnomAD v2: X-66765161-A-T
• gnomAD v3: X-67545319-A-T
• gnomAD v4: X-67545319-A-T
• MyVariant Identifiers: chrX:g.66765161A>T (hg19) ; chrX:g.66765161_66765162delinsTG (hg19) ; chrX:g.67545319A>T (hg38) ; chrX:g.67545319_67545320delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545319A>T , CM000685.2:g.67545319A>T	GRCh38
NC_000023.10:g.66765161A>T , CM000685.1:g.66765161A>T	GRCh37
NC_000023.9:g.66681886A>T	NCBI36
NG_009014.2:g.6288A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.173A>T	ENSP00000379358.4:p.Gln58Leu
ENST00000374690.9:c.173A>T MANE Select	ENSP00000363822.3:p.Gln58Leu
ENST00000396044.8:c.173A>T	ENSP00000379359.3:p.Gln58Leu
ENST00000612452.5:c.173A>T	ENSP00000484033.2:p.Gln58Leu
ENST00000374690.7:c.173A>T	ENSP00000363822.3:p.Gln58Leu
ENST00000396044.7:c.173A>T	ENSP00000379359.3:p.Gln58Leu
ENST00000504326.5:c.173A>T	ENSP00000421155.1:p.Gln58Leu
ENST00000513847.5:n.500A>T
ENST00000514029.5:c.173A>T	ENSP00000425199.1:p.Gln58Leu
ENST00000612010.4:c.173A>T	ENSP00000482407.1:p.Gln58Leu
ENST00000612452.4:c.-398A>T	ENSP00000484033.1:n.-398A>T
ENST00000613054.2:c.173A>T	ENSP00000479013.1:p.Gln58Leu
NM_000044.3:c.173A>T	NP_000035.2:p.Gln58Leu
NM_000044.4:c.173A>T	NP_000035.2:p.Gln58Leu
NM_001011645.3:c.-1611A>T	NP_001011645.1:n.-1611A>T
NM_001348061.1:c.173A>T	NP_001334990.1:p.Gln58Leu
NM_001348063.1:c.173A>T	NP_001334992.1:p.Gln58Leu
NM_001348064.1:c.173A>T	NP_001334993.1:p.Gln58Leu
NM_000044.6:c.173A>T MANE Select	NP_000035.2:p.Gln58Leu