Canonical Allele Identifier: CA413423567

Gene: AR

Linked Data

• ClinVar Variation Id: 1077100
• ClinVar RCV Id: RCV001391228
• dbSNP Id: rs2147525357
• MyVariant Identifiers: chrX:g.66931528C>T (hg19) ; chrX:g.67711686C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711686C>T , CM000685.2:g.67711686C>T	GRCh38
NC_000023.10:g.66931528C>T , CM000685.1:g.66931528C>T	GRCh37
NC_000023.9:g.66848253C>T	NCBI36
NG_009014.2:g.172655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*518C>T	ENSP00000379358.4:n.*518C>T
ENST00000374690.9:c.2170C>T MANE Select	ENSP00000363822.3:p.Pro724Ser
ENST00000396043.3:c.797C>T	ENSP00000379358.3:n.797C>T
ENST00000396044.8:c.2170C>T	ENSP00000379359.3:p.Pro724Ser
ENST00000612452.5:c.2170C>T	ENSP00000484033.2:p.Pro724Ser
ENST00000374690.7:c.2170C>T	ENSP00000363822.3:p.Pro724Ser
ENST00000396043.2:c.574C>T	ENSP00000379358.2:p.Pro192Ser
ENST00000396044.7:c.2170C>T	ENSP00000379359.3:p.Pro724Ser
ENST00000612452.4:c.1600C>T	ENSP00000484033.1:p.Pro534Ser
NM_000044.3:c.2170C>T	NP_000035.2:p.Pro724Ser
NM_001011645.2:c.574C>T	NP_001011645.1:p.Pro192Ser
NM_000044.4:c.2170C>T	NP_000035.2:p.Pro724Ser
NM_001011645.3:c.574C>T	NP_001011645.1:p.Pro192Ser
NM_000044.6:c.2170C>T MANE Select	NP_000035.2:p.Pro724Ser