Canonical Allele Identifier: CA413428257

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66943577A>C (hg19) ; chrX:g.67723735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723735A>C , CM000685.2:g.67723735A>C	GRCh38
NC_000023.10:g.66943577A>C , CM000685.1:g.66943577A>C	GRCh37
NC_000023.9:g.66860302A>C	NCBI36
NG_009014.2:g.184704A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1005A>C	ENSP00000379358.4:n.*1005A>C
ENST00000374690.9:c.2657A>C MANE Select	ENSP00000363822.3:p.His886Pro
ENST00000396043.3:c.1284A>C	ENSP00000379358.3:n.1284A>C
ENST00000396044.8:c.*18A>C	ENSP00000379359.3:n.*18A>C
ENST00000612452.5:c.2657A>C	ENSP00000484033.2:p.His886Pro
ENST00000374690.7:c.2657A>C	ENSP00000363822.3:p.His886Pro
ENST00000396043.2:c.1061A>C	ENSP00000379358.2:p.His354Pro
ENST00000396044.7:c.*18A>C	ENSP00000379359.3:n.*18A>C
ENST00000612452.4:c.2108A>C	ENSP00000484033.1:p.His703Pro
NM_000044.3:c.2657A>C	NP_000035.2:p.His886Pro
NM_001011645.2:c.1061A>C	NP_001011645.1:p.His354Pro
NM_000044.4:c.2657A>C	NP_000035.2:p.His886Pro
NM_001011645.3:c.1061A>C	NP_001011645.1:p.His354Pro
NM_000044.6:c.2657A>C MANE Select	NP_000035.2:p.His886Pro