Canonical Allele Identifier: CA517047760

Gene: AR

Linked Data

• ClinVar Variation Id: 2942475
• ClinVar RCV Id: RCV003805689
• dbSNP Id: rs752559194
• gnomAD v4: X-67545605-G-C
• MyVariant Identifiers: chrX:g.66765447G>C (hg19) ; chrX:g.67545605G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545605G>C , CM000685.2:g.67545605G>C	GRCh38
NC_000023.10:g.66765447G>C , CM000685.1:g.66765447G>C	GRCh37
NC_000023.9:g.66682172G>C	NCBI36
NG_009014.2:g.6574G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.459G>C	ENSP00000379358.4:p.Pro153=
ENST00000374690.9:c.459G>C MANE Select	ENSP00000363822.3:p.Pro153=
ENST00000396044.8:c.459G>C	ENSP00000379359.3:p.Pro153=
ENST00000612452.5:c.459G>C	ENSP00000484033.2:p.Pro153=
ENST00000374690.7:c.459G>C	ENSP00000363822.3:p.Pro153=
ENST00000396044.7:c.459G>C	ENSP00000379359.3:p.Pro153=
ENST00000504326.5:c.459G>C	ENSP00000421155.1:p.Pro153=
ENST00000513847.5:n.786G>C
ENST00000514029.5:c.459G>C	ENSP00000425199.1:p.Pro153=
ENST00000612010.4:c.459G>C	ENSP00000482407.1:p.Pro153=
ENST00000612452.4:c.-112G>C	ENSP00000484033.1:n.-112G>C
ENST00000613054.2:c.459G>C	ENSP00000479013.1:p.Pro153=
NM_000044.3:c.459G>C	NP_000035.2:p.Pro153=
NM_000044.4:c.459G>C	NP_000035.2:p.Pro153=
NM_001011645.3:c.-1325G>C	NP_001011645.1:n.-1325G>C
NM_001348061.1:c.459G>C	NP_001334990.1:p.Pro153=
NM_001348063.1:c.459G>C	NP_001334992.1:p.Pro153=
NM_001348064.1:c.459G>C	NP_001334993.1:p.Pro153=
NM_000044.6:c.459G>C MANE Select	NP_000035.2:p.Pro153=