Canonical Allele Identifier: CA516971676

Gene: AR

Linked Data

• dbSNP Id: rs2147537677
• MyVariant Identifiers: chrX:g.66942673A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722831A>G , CM000685.2:g.67722831A>G	GRCh38
NC_000023.10:g.66942673A>G , CM000685.1:g.66942673A>G	GRCh37
NC_000023.9:g.66859398A>G	NCBI36
NG_009014.2:g.183800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*802A>G	ENSP00000379358.4:n.*802A>G
ENST00000374690.9:c.2454A>G MANE Select	ENSP00000363822.3:p.Pro818=
ENST00000396043.3:c.1081A>G	ENSP00000379358.3:n.1081A>G
ENST00000396044.8:c.2174-855A>G	ENSP00000379359.3:n.2174-855A>G
ENST00000612452.5:c.2454A>G	ENSP00000484033.2:p.Pro818=
ENST00000374690.7:c.2454A>G	ENSP00000363822.3:p.Pro818=
ENST00000396043.2:c.858A>G	ENSP00000379358.2:p.Pro286=
ENST00000396044.7:c.2174-855A>G	ENSP00000379359.3:n.2174-855A>G
ENST00000612452.4:c.1905A>G	ENSP00000484033.1:p.Pro635=
NM_000044.3:c.2454A>G	NP_000035.2:p.Pro818=
NM_001011645.2:c.858A>G	NP_001011645.1:p.Pro286=
NM_000044.4:c.2454A>G	NP_000035.2:p.Pro818=
NM_001011645.3:c.858A>G	NP_001011645.1:p.Pro286=
NM_000044.6:c.2454A>G MANE Select	NP_000035.2:p.Pro818=