Canonical Allele Identifier: CA516973485

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66905931T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686089T>G , CM000685.2:g.67686089T>G	GRCh38
NC_000023.10:g.66905931T>G , CM000685.1:g.66905931T>G	GRCh37
NC_000023.9:g.66822656T>G	NCBI36
NG_009014.2:g.147058T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*196T>G	ENSP00000379358.4:n.*196T>G
ENST00000374690.9:c.1848T>G MANE Select	ENSP00000363822.3:p.Arg616=
ENST00000396043.3:c.475T>G	ENSP00000379358.3:n.475T>G
ENST00000396044.8:c.1848T>G	ENSP00000379359.3:p.Arg616=
ENST00000612452.5:c.1848T>G	ENSP00000484033.2:p.Arg616=
ENST00000374690.7:c.1848T>G	ENSP00000363822.3:p.Arg616=
ENST00000396043.2:c.252T>G	ENSP00000379358.2:p.Arg84=
ENST00000396044.7:c.1848T>G	ENSP00000379359.3:p.Arg616=
ENST00000504326.5:c.1848T>G	ENSP00000421155.1:p.Arg616=
ENST00000513847.5:n.2175T>G
ENST00000514029.5:c.*329T>G	ENSP00000425199.1:n.*329T>G
ENST00000612010.4:c.*200T>G	ENSP00000482407.1:n.*200T>G
ENST00000612452.4:c.1278T>G	ENSP00000484033.1:p.Arg426=
ENST00000613054.2:c.*46T>G	ENSP00000479013.1:n.*46T>G
NM_000044.3:c.1848T>G	NP_000035.2:p.Arg616=
NM_001011645.2:c.252T>G	NP_001011645.1:p.Arg84=
NM_000044.4:c.1848T>G	NP_000035.2:p.Arg616=
NM_001011645.3:c.252T>G	NP_001011645.1:p.Arg84=
NM_001348061.1:c.1848T>G	NP_001334990.1:p.Arg616=
NM_001348063.1:c.1848T>G	NP_001334992.1:p.Arg616=
NM_001348064.1:c.*46T>G	NP_001334993.1:n.*46T>G
NM_000044.6:c.1848T>G MANE Select	NP_000035.2:p.Arg616=