Canonical Allele Identifier: CA413423070

Gene: AR

Linked Data

• dbSNP Id: rs2076093337
• MyVariant Identifiers: chrX:g.66931300A>T (hg19) ; chrX:g.67711458A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711458A>T , CM000685.2:g.67711458A>T	GRCh38
NC_000023.10:g.66931300A>T , CM000685.1:g.66931300A>T	GRCh37
NC_000023.9:g.66848025A>T	NCBI36
NG_009014.2:g.172427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*290A>T	ENSP00000379358.4:n.*290A>T
ENST00000374690.9:c.1942A>T MANE Select	ENSP00000363822.3:p.Ser648Cys
ENST00000396043.3:c.569A>T	ENSP00000379358.3:n.569A>T
ENST00000396044.8:c.1942A>T	ENSP00000379359.3:p.Ser648Cys
ENST00000612452.5:c.1942A>T	ENSP00000484033.2:p.Ser648Cys
ENST00000374690.7:c.1942A>T	ENSP00000363822.3:p.Ser648Cys
ENST00000396043.2:c.346A>T	ENSP00000379358.2:p.Ser116Cys
ENST00000396044.7:c.1942A>T	ENSP00000379359.3:p.Ser648Cys
ENST00000612452.4:c.1372A>T	ENSP00000484033.1:p.Ser458Cys
NM_000044.3:c.1942A>T	NP_000035.2:p.Ser648Cys
NM_001011645.2:c.346A>T	NP_001011645.1:p.Ser116Cys
NM_000044.4:c.1942A>T	NP_000035.2:p.Ser648Cys
NM_001011645.3:c.346A>T	NP_001011645.1:p.Ser116Cys
NM_000044.6:c.1942A>T MANE Select	NP_000035.2:p.Ser648Cys