Canonical Allele Identifier: CA413427988

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942762A>T (hg19) ; chrX:g.67722920A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722920A>T , CM000685.2:g.67722920A>T	GRCh38
NC_000023.10:g.66942762A>T , CM000685.1:g.66942762A>T	GRCh37
NC_000023.9:g.66859487A>T	NCBI36
NG_009014.2:g.183889A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*891A>T	ENSP00000379358.4:n.*891A>T
ENST00000374690.9:c.2543A>T MANE Select	ENSP00000363822.3:p.Lys848Ile
ENST00000396043.3:c.1170A>T	ENSP00000379358.3:n.1170A>T
ENST00000396044.8:c.2174-766A>T	ENSP00000379359.3:n.2174-766A>T
ENST00000612452.5:c.2543A>T	ENSP00000484033.2:p.Lys848Ile
ENST00000374690.7:c.2543A>T	ENSP00000363822.3:p.Lys848Ile
ENST00000396043.2:c.947A>T	ENSP00000379358.2:p.Lys316Ile
ENST00000396044.7:c.2174-766A>T	ENSP00000379359.3:n.2174-766A>T
ENST00000612452.4:c.1994A>T	ENSP00000484033.1:p.Lys665Ile
NM_000044.3:c.2543A>T	NP_000035.2:p.Lys848Ile
NM_001011645.2:c.947A>T	NP_001011645.1:p.Lys316Ile
NM_000044.4:c.2543A>T	NP_000035.2:p.Lys848Ile
NM_001011645.3:c.947A>T	NP_001011645.1:p.Lys316Ile
NM_000044.6:c.2543A>T MANE Select	NP_000035.2:p.Lys848Ile