Canonical Allele Identifier: CA517048428

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66931434C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711592C>T , CM000685.2:g.67711592C>T	GRCh38
NC_000023.10:g.66931434C>T , CM000685.1:g.66931434C>T	GRCh37
NC_000023.9:g.66848159C>T	NCBI36
NG_009014.2:g.172561C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*424C>T	ENSP00000379358.4:n.*424C>T
ENST00000374690.9:c.2076C>T MANE Select	ENSP00000363822.3:p.Asn692=
ENST00000396043.3:c.703C>T	ENSP00000379358.3:n.703C>T
ENST00000396044.8:c.2076C>T	ENSP00000379359.3:p.Asn692=
ENST00000612452.5:c.2076C>T	ENSP00000484033.2:p.Asn692=
ENST00000374690.7:c.2076C>T	ENSP00000363822.3:p.Asn692=
ENST00000396043.2:c.480C>T	ENSP00000379358.2:p.Asn160=
ENST00000396044.7:c.2076C>T	ENSP00000379359.3:p.Asn692=
ENST00000612452.4:c.1506C>T	ENSP00000484033.1:p.Asn502=
NM_000044.3:c.2076C>T	NP_000035.2:p.Asn692=
NM_001011645.2:c.480C>T	NP_001011645.1:p.Asn160=
NM_000044.4:c.2076C>T	NP_000035.2:p.Asn692=
NM_001011645.3:c.480C>T	NP_001011645.1:p.Asn160=
NM_000044.6:c.2076C>T MANE Select	NP_000035.2:p.Asn692=