Canonical Allele Identifier: CA413426453

Gene: AR

Linked Data

• ClinVar Variation Id: 2674671
• ClinVar RCV Id: RCV003459915
• dbSNP Id: rs768366293
• MyVariant Identifiers: chrX:g.66941695G>C (hg19) ; chrX:g.67721853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721853G>C , CM000685.2:g.67721853G>C	GRCh38
NC_000023.10:g.66941695G>C , CM000685.1:g.66941695G>C	GRCh37
NC_000023.9:g.66858420G>C	NCBI36
NG_009014.2:g.182822G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*687G>C	ENSP00000379358.4:n.*687G>C
ENST00000374690.9:c.2339G>C MANE Select	ENSP00000363822.3:p.Arg780Pro
ENST00000396043.3:c.966G>C	ENSP00000379358.3:n.966G>C
ENST00000396044.8:c.2174-1833G>C	ENSP00000379359.3:n.2174-1833G>C
ENST00000612452.5:c.2339G>C	ENSP00000484033.2:p.Arg780Pro
ENST00000374690.7:c.2339G>C	ENSP00000363822.3:p.Arg780Pro
ENST00000396043.2:c.743G>C	ENSP00000379358.2:p.Arg248Pro
ENST00000396044.7:c.2174-1833G>C	ENSP00000379359.3:n.2174-1833G>C
ENST00000612452.4:c.1769G>C	ENSP00000484033.1:p.Arg590Pro
NM_000044.3:c.2339G>C	NP_000035.2:p.Arg780Pro
NM_001011645.2:c.743G>C	NP_001011645.1:p.Arg248Pro
NM_000044.4:c.2339G>C	NP_000035.2:p.Arg780Pro
NM_001011645.3:c.743G>C	NP_001011645.1:p.Arg248Pro
NM_000044.6:c.2339G>C MANE Select	NP_000035.2:p.Arg780Pro