Canonical Allele Identifier: CA413426428

Gene: AR

Linked Data

• ClinVar Variation Id: 1025856
• ClinVar RCV Id: RCV001326231 ; RCV003135982
• dbSNP Id: rs2076137260
• MyVariant Identifiers: chrX:g.66941690G>T (hg19) ; chrX:g.67721848G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721848G>T , CM000685.2:g.67721848G>T	GRCh38
NC_000023.10:g.66941690G>T , CM000685.1:g.66941690G>T	GRCh37
NC_000023.9:g.66858415G>T	NCBI36
NG_009014.2:g.182817G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*682G>T	ENSP00000379358.4:n.*682G>T
ENST00000374690.9:c.2334G>T MANE Select	ENSP00000363822.3:p.Lys778Asn
ENST00000396043.3:c.961G>T	ENSP00000379358.3:n.961G>T
ENST00000396044.8:c.2174-1838G>T	ENSP00000379359.3:n.2174-1838G>T
ENST00000612452.5:c.2334G>T	ENSP00000484033.2:p.Lys778Asn
ENST00000374690.7:c.2334G>T	ENSP00000363822.3:p.Lys778Asn
ENST00000396043.2:c.738G>T	ENSP00000379358.2:p.Lys246Asn
ENST00000396044.7:c.2174-1838G>T	ENSP00000379359.3:n.2174-1838G>T
ENST00000612452.4:c.1764G>T	ENSP00000484033.1:p.Lys588Asn
NM_000044.3:c.2334G>T	NP_000035.2:p.Lys778Asn
NM_001011645.2:c.738G>T	NP_001011645.1:p.Lys246Asn
NM_000044.4:c.2334G>T	NP_000035.2:p.Lys778Asn
NM_001011645.3:c.738G>T	NP_001011645.1:p.Lys246Asn
NM_000044.6:c.2334G>T MANE Select	NP_000035.2:p.Lys778Asn