Canonical Allele Identifier: CA413429273

Gene: AR

Linked Data

• ClinVar Variation Id: 988308
• ClinVar RCV Id: RCV001269573
• dbSNP Id: rs2075964906
• MyVariant Identifiers: chrX:g.66905916T>A (hg19) ; chrX:g.67686074T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686074T>A , CM000685.2:g.67686074T>A	GRCh38
NC_000023.10:g.66905916T>A , CM000685.1:g.66905916T>A	GRCh37
NC_000023.9:g.66822641T>A	NCBI36
NG_009014.2:g.147043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*181T>A	ENSP00000379358.4:n.*181T>A
ENST00000374690.9:c.1833T>A MANE Select	ENSP00000363822.3:p.Asn611Lys
ENST00000396043.3:c.460T>A	ENSP00000379358.3:n.460T>A
ENST00000396044.8:c.1833T>A	ENSP00000379359.3:p.Asn611Lys
ENST00000612452.5:c.1833T>A	ENSP00000484033.2:p.Asn611Lys
ENST00000374690.7:c.1833T>A	ENSP00000363822.3:p.Asn611Lys
ENST00000396043.2:c.237T>A	ENSP00000379358.2:p.Asn79Lys
ENST00000396044.7:c.1833T>A	ENSP00000379359.3:p.Asn611Lys
ENST00000504326.5:c.1833T>A	ENSP00000421155.1:p.Asn611Lys
ENST00000513847.5:n.2160T>A
ENST00000514029.5:c.*314T>A	ENSP00000425199.1:n.*314T>A
ENST00000612010.4:c.*185T>A	ENSP00000482407.1:n.*185T>A
ENST00000612452.4:c.1263T>A	ENSP00000484033.1:p.Asn421Lys
ENST00000613054.2:c.*31T>A	ENSP00000479013.1:n.*31T>A
NM_000044.3:c.1833T>A	NP_000035.2:p.Asn611Lys
NM_001011645.2:c.237T>A	NP_001011645.1:p.Asn79Lys
NM_000044.4:c.1833T>A	NP_000035.2:p.Asn611Lys
NM_001011645.3:c.237T>A	NP_001011645.1:p.Asn79Lys
NM_001348061.1:c.1833T>A	NP_001334990.1:p.Asn611Lys
NM_001348063.1:c.1833T>A	NP_001334992.1:p.Asn611Lys
NM_001348064.1:c.*31T>A	NP_001334993.1:n.*31T>A
NM_000044.6:c.1833T>A MANE Select	NP_000035.2:p.Asn611Lys