Canonical Allele Identifier: CA10436392

Gene: AR

Linked Data

• ClinVar Variation Id: 2947102
• ClinVar RCV Id: RCV003801292
• dbSNP Id: rs555361360
• ExAC: X:66766145 G / A
• gnomAD v2: X-66766145-G-A
• gnomAD v3: X-67546303-G-A
• gnomAD v4: X-67546303-G-A
• MyVariant Identifiers: chrX:g.66766145G>A (hg19) ; chrX:g.67546303G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67546303G>A , CM000685.2:g.67546303G>A	GRCh38
NC_000023.10:g.66766145G>A , CM000685.1:g.66766145G>A	GRCh37
NC_000023.9:g.66682870G>A	NCBI36
NG_009014.2:g.7272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.1157G>A	ENSP00000379358.4:p.Arg386His
ENST00000374690.9:c.1157G>A MANE Select	ENSP00000363822.3:p.Arg386His
ENST00000396044.8:c.1157G>A	ENSP00000379359.3:p.Arg386His
ENST00000612452.5:c.1157G>A	ENSP00000484033.2:p.Arg386His
ENST00000374690.7:c.1157G>A	ENSP00000363822.3:p.Arg386His
ENST00000396044.7:c.1157G>A	ENSP00000379359.3:p.Arg386His
ENST00000504326.5:c.1157G>A	ENSP00000421155.1:p.Arg386His
ENST00000513847.5:n.1484G>A
ENST00000514029.5:c.1157G>A	ENSP00000425199.1:p.Arg386His
ENST00000612010.4:c.1157G>A	ENSP00000482407.1:p.Arg386His
ENST00000612452.4:c.587G>A	ENSP00000484033.1:p.Arg196His
ENST00000613054.2:c.1157G>A	ENSP00000479013.1:p.Arg386His
NM_000044.3:c.1157G>A	NP_000035.2:p.Arg386His
NM_000044.4:c.1157G>A	NP_000035.2:p.Arg386His
NM_001011645.3:c.-627G>A	NP_001011645.1:n.-627G>A
NM_001348061.1:c.1157G>A	NP_001334990.1:p.Arg386His
NM_001348063.1:c.1157G>A	NP_001334992.1:p.Arg386His
NM_001348064.1:c.1157G>A	NP_001334993.1:p.Arg386His
NM_000044.6:c.1157G>A MANE Select	NP_000035.2:p.Arg386His