Canonical Allele Identifier: CA413426824

Gene: AR

Linked Data

• dbSNP Id: rs2147535880
• MyVariant Identifiers: chrX:g.66941755T>A (hg19) ; chrX:g.67721913T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721913T>A , CM000685.2:g.67721913T>A	GRCh38
NC_000023.10:g.66941755T>A , CM000685.1:g.66941755T>A	GRCh37
NC_000023.9:g.66858480T>A	NCBI36
NG_009014.2:g.182882T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*747T>A	ENSP00000379358.4:n.*747T>A
ENST00000374690.9:c.2399T>A MANE Select	ENSP00000363822.3:p.Ile800Asn
ENST00000396043.3:c.1026T>A	ENSP00000379358.3:n.1026T>A
ENST00000396044.8:c.2174-1773T>A	ENSP00000379359.3:n.2174-1773T>A
ENST00000612452.5:c.2399T>A	ENSP00000484033.2:p.Ile800Asn
ENST00000374690.7:c.2399T>A	ENSP00000363822.3:p.Ile800Asn
ENST00000396043.2:c.803T>A	ENSP00000379358.2:p.Ile268Asn
ENST00000396044.7:c.2174-1773T>A	ENSP00000379359.3:n.2174-1773T>A
ENST00000612452.4:c.1829T>A	ENSP00000484033.1:p.Ile610Asn
NM_000044.3:c.2399T>A	NP_000035.2:p.Ile800Asn
NM_001011645.2:c.803T>A	NP_001011645.1:p.Ile268Asn
NM_000044.4:c.2399T>A	NP_000035.2:p.Ile800Asn
NM_001011645.3:c.803T>A	NP_001011645.1:p.Ile268Asn
NM_000044.6:c.2399T>A MANE Select	NP_000035.2:p.Ile800Asn