Canonical Allele Identifier: CA516973481

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66905925T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686083T>G , CM000685.2:g.67686083T>G	GRCh38
NC_000023.10:g.66905925T>G , CM000685.1:g.66905925T>G	GRCh37
NC_000023.9:g.66822650T>G	NCBI36
NG_009014.2:g.147052T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*190T>G	ENSP00000379358.4:n.*190T>G
ENST00000374690.9:c.1842T>G MANE Select	ENSP00000363822.3:p.Ser614=
ENST00000396043.3:c.469T>G	ENSP00000379358.3:n.469T>G
ENST00000396044.8:c.1842T>G	ENSP00000379359.3:p.Ser614=
ENST00000612452.5:c.1842T>G	ENSP00000484033.2:p.Ser614=
ENST00000374690.7:c.1842T>G	ENSP00000363822.3:p.Ser614=
ENST00000396043.2:c.246T>G	ENSP00000379358.2:p.Ser82=
ENST00000396044.7:c.1842T>G	ENSP00000379359.3:p.Ser614=
ENST00000504326.5:c.1842T>G	ENSP00000421155.1:p.Ser614=
ENST00000513847.5:n.2169T>G
ENST00000514029.5:c.*323T>G	ENSP00000425199.1:n.*323T>G
ENST00000612010.4:c.*194T>G	ENSP00000482407.1:n.*194T>G
ENST00000612452.4:c.1272T>G	ENSP00000484033.1:p.Ser424=
ENST00000613054.2:c.*40T>G	ENSP00000479013.1:n.*40T>G
NM_000044.3:c.1842T>G	NP_000035.2:p.Ser614=
NM_001011645.2:c.246T>G	NP_001011645.1:p.Ser82=
NM_000044.4:c.1842T>G	NP_000035.2:p.Ser614=
NM_001011645.3:c.246T>G	NP_001011645.1:p.Ser82=
NM_001348061.1:c.1842T>G	NP_001334990.1:p.Ser614=
NM_001348063.1:c.1842T>G	NP_001334992.1:p.Ser614=
NM_001348064.1:c.*40T>G	NP_001334993.1:n.*40T>G
NM_000044.6:c.1842T>G MANE Select	NP_000035.2:p.Ser614=