Canonical Allele Identifier: CA516970816

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66941744A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721902A>C , CM000685.2:g.67721902A>C	GRCh38
NC_000023.10:g.66941744A>C , CM000685.1:g.66941744A>C	GRCh37
NC_000023.9:g.66858469A>C	NCBI36
NG_009014.2:g.182871A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*736A>C	ENSP00000379358.4:n.*736A>C
ENST00000374690.9:c.2388A>C MANE Select	ENSP00000363822.3:p.Gly796=
ENST00000396043.3:c.1015A>C	ENSP00000379358.3:n.1015A>C
ENST00000396044.8:c.2174-1784A>C	ENSP00000379359.3:n.2174-1784A>C
ENST00000612452.5:c.2388A>C	ENSP00000484033.2:p.Gly796=
ENST00000374690.7:c.2388A>C	ENSP00000363822.3:p.Gly796=
ENST00000396043.2:c.792A>C	ENSP00000379358.2:p.Gly264=
ENST00000396044.7:c.2174-1784A>C	ENSP00000379359.3:n.2174-1784A>C
ENST00000612452.4:c.1818A>C	ENSP00000484033.1:p.Gly606=
NM_000044.3:c.2388A>C	NP_000035.2:p.Gly796=
NM_001011645.2:c.792A>C	NP_001011645.1:p.Gly264=
NM_000044.4:c.2388A>C	NP_000035.2:p.Gly796=
NM_001011645.3:c.792A>C	NP_001011645.1:p.Gly264=
NM_000044.6:c.2388A>C MANE Select	NP_000035.2:p.Gly796=