Canonical Allele Identifier: CA413429352

Gene: AR

Linked Data

• dbSNP Id: rs2147497900
• MyVariant Identifiers: chrX:g.66905951C>T (hg19) ; chrX:g.67686109C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686109C>T , CM000685.2:g.67686109C>T	GRCh38
NC_000023.10:g.66905951C>T , CM000685.1:g.66905951C>T	GRCh37
NC_000023.9:g.66822676C>T	NCBI36
NG_009014.2:g.147078C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*216C>T	ENSP00000379358.4:n.*216C>T
ENST00000374690.9:c.1868C>T MANE Select	ENSP00000363822.3:p.Ala623Val
ENST00000396043.3:c.495C>T	ENSP00000379358.3:n.495C>T
ENST00000396044.8:c.1868C>T	ENSP00000379359.3:p.Ala623Val
ENST00000612452.5:c.1868C>T	ENSP00000484033.2:p.Ala623Val
ENST00000374690.7:c.1868C>T	ENSP00000363822.3:p.Ala623Val
ENST00000396043.2:c.272C>T	ENSP00000379358.2:p.Ala91Val
ENST00000396044.7:c.1868C>T	ENSP00000379359.3:p.Ala623Val
ENST00000504326.5:c.1868C>T	ENSP00000421155.1:p.Ala623Val
ENST00000513847.5:n.2195C>T
ENST00000514029.5:c.*349C>T	ENSP00000425199.1:n.*349C>T
ENST00000612010.4:c.*220C>T	ENSP00000482407.1:n.*220C>T
ENST00000612452.4:c.1298C>T	ENSP00000484033.1:p.Ala433Val
ENST00000613054.2:c.*66C>T	ENSP00000479013.1:n.*66C>T
NM_000044.3:c.1868C>T	NP_000035.2:p.Ala623Val
NM_001011645.2:c.272C>T	NP_001011645.1:p.Ala91Val
NM_000044.4:c.1868C>T	NP_000035.2:p.Ala623Val
NM_001011645.3:c.272C>T	NP_001011645.1:p.Ala91Val
NM_001348061.1:c.1868C>T	NP_001334990.1:p.Ala623Val
NM_001348063.1:c.1868C>T	NP_001334992.1:p.Ala623Val
NM_001348064.1:c.*66C>T	NP_001334993.1:n.*66C>T
NM_000044.6:c.1868C>T MANE Select	NP_000035.2:p.Ala623Val