Canonical Allele Identifier: CA413426388

Gene: AR

Linked Data

• ClinVar Variation Id: 2102759
• ClinVar RCV Id: RCV003019671
• dbSNP Id: rs2147535523
• MyVariant Identifiers: chrX:g.66941683T>C (hg19) ; chrX:g.67721841T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721841T>C , CM000685.2:g.67721841T>C	GRCh38
NC_000023.10:g.66941683T>C , CM000685.1:g.66941683T>C	GRCh37
NC_000023.9:g.66858408T>C	NCBI36
NG_009014.2:g.182810T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*675T>C	ENSP00000379358.4:n.*675T>C
ENST00000374690.9:c.2327T>C MANE Select	ENSP00000363822.3:p.Met776Thr
ENST00000396043.3:c.954T>C	ENSP00000379358.3:n.954T>C
ENST00000396044.8:c.2174-1845T>C	ENSP00000379359.3:n.2174-1845T>C
ENST00000612452.5:c.2327T>C	ENSP00000484033.2:p.Met776Thr
ENST00000374690.7:c.2327T>C	ENSP00000363822.3:p.Met776Thr
ENST00000396043.2:c.731T>C	ENSP00000379358.2:p.Met244Thr
ENST00000396044.7:c.2174-1845T>C	ENSP00000379359.3:n.2174-1845T>C
ENST00000612452.4:c.1757T>C	ENSP00000484033.1:p.Met586Thr
NM_000044.3:c.2327T>C	NP_000035.2:p.Met776Thr
NM_001011645.2:c.731T>C	NP_001011645.1:p.Met244Thr
NM_000044.4:c.2327T>C	NP_000035.2:p.Met776Thr
NM_001011645.3:c.731T>C	NP_001011645.1:p.Met244Thr
NM_000044.6:c.2327T>C MANE Select	NP_000035.2:p.Met776Thr