Canonical Allele Identifier: CA413428462

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66943664T>C (hg19) ; chrX:g.67723822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723822T>C , CM000685.2:g.67723822T>C	GRCh38
NC_000023.10:g.66943664T>C , CM000685.1:g.66943664T>C	GRCh37
NC_000023.9:g.66860389T>C	NCBI36
NG_009014.2:g.184791T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1092T>C	ENSP00000379358.4:n.*1092T>C
ENST00000374690.9:c.2744T>C MANE Select	ENSP00000363822.3:p.Ile915Thr
ENST00000396043.3:c.1371T>C	ENSP00000379358.3:n.1371T>C
ENST00000396044.8:c.*105T>C	ENSP00000379359.3:n.*105T>C
ENST00000612452.5:c.2744T>C	ENSP00000484033.2:p.Ile915Thr
ENST00000374690.7:c.2744T>C	ENSP00000363822.3:p.Ile915Thr
ENST00000396043.2:c.1148T>C	ENSP00000379358.2:p.Ile383Thr
ENST00000396044.7:c.*105T>C	ENSP00000379359.3:n.*105T>C
ENST00000612452.4:c.2195T>C	ENSP00000484033.1:p.Ile732Thr
NM_000044.3:c.2744T>C	NP_000035.2:p.Ile915Thr
NM_001011645.2:c.1148T>C	NP_001011645.1:p.Ile383Thr
NM_000044.4:c.2744T>C	NP_000035.2:p.Ile915Thr
NM_001011645.3:c.1148T>C	NP_001011645.1:p.Ile383Thr
NM_000044.6:c.2744T>C MANE Select	NP_000035.2:p.Ile915Thr