Canonical Allele Identifier: CA413423147

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66931335G>T (hg19) ; chrX:g.67711493G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711493G>T , CM000685.2:g.67711493G>T	GRCh38
NC_000023.10:g.66931335G>T , CM000685.1:g.66931335G>T	GRCh37
NC_000023.9:g.66848060G>T	NCBI36
NG_009014.2:g.172462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*325G>T	ENSP00000379358.4:n.*325G>T
ENST00000374690.9:c.1977G>T MANE Select	ENSP00000363822.3:p.Lys659Asn
ENST00000396043.3:c.604G>T	ENSP00000379358.3:n.604G>T
ENST00000396044.8:c.1977G>T	ENSP00000379359.3:p.Lys659Asn
ENST00000612452.5:c.1977G>T	ENSP00000484033.2:p.Lys659Asn
ENST00000374690.7:c.1977G>T	ENSP00000363822.3:p.Lys659Asn
ENST00000396043.2:c.381G>T	ENSP00000379358.2:p.Lys127Asn
ENST00000396044.7:c.1977G>T	ENSP00000379359.3:p.Lys659Asn
ENST00000612452.4:c.1407G>T	ENSP00000484033.1:p.Lys469Asn
NM_000044.3:c.1977G>T	NP_000035.2:p.Lys659Asn
NM_001011645.2:c.381G>T	NP_001011645.1:p.Lys127Asn
NM_000044.4:c.1977G>T	NP_000035.2:p.Lys659Asn
NM_001011645.3:c.381G>T	NP_001011645.1:p.Lys127Asn
NM_000044.6:c.1977G>T MANE Select	NP_000035.2:p.Lys659Asn