Canonical Allele Identifier: CA413422968

Gene: AR

Linked Data

• ClinVar Variation Id: 650823
• ClinVar RCV Id: RCV000806051
• dbSNP Id: rs1602272308
• MyVariant Identifiers: chrX:g.66931255A>T (hg19) ; chrX:g.67711413A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711413A>T , CM000685.2:g.67711413A>T	GRCh38
NC_000023.10:g.66931255A>T , CM000685.1:g.66931255A>T	GRCh37
NC_000023.9:g.66847980A>T	NCBI36
NG_009014.2:g.172382A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*245A>T	ENSP00000379358.4:n.*245A>T
ENST00000374690.9:c.1897A>T MANE Select	ENSP00000363822.3:p.Lys633Ter
ENST00000396043.3:c.524A>T	ENSP00000379358.3:n.524A>T
ENST00000396044.8:c.1897A>T	ENSP00000379359.3:p.Lys633Ter
ENST00000612452.5:c.1897A>T	ENSP00000484033.2:p.Lys633Ter
ENST00000374690.7:c.1897A>T	ENSP00000363822.3:p.Lys633Ter
ENST00000396043.2:c.301A>T	ENSP00000379358.2:p.Lys101Ter
ENST00000396044.7:c.1897A>T	ENSP00000379359.3:p.Lys633Ter
ENST00000612452.4:c.1327A>T	ENSP00000484033.1:p.Lys443Ter
NM_000044.3:c.1897A>T	NP_000035.2:p.Lys633Ter
NM_001011645.2:c.301A>T	NP_001011645.1:p.Lys101Ter
NM_000044.4:c.1897A>T	NP_000035.2:p.Lys633Ter
NM_001011645.3:c.301A>T	NP_001011645.1:p.Lys101Ter
NM_000044.6:c.1897A>T MANE Select	NP_000035.2:p.Lys633Ter