Canonical Allele Identifier: CA10436574

Gene: AR

Linked Data

• dbSNP Id: rs372903533
• ExAC: X:66931441 C / T
• gnomAD v2: X-66931441-C-T
• gnomAD v3: X-67711599-C-T
• gnomAD v4: X-67711599-C-T
• MyVariant Identifiers: chrX:g.66931441C>T (hg19) ; chrX:g.67711599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711599C>T , CM000685.2:g.67711599C>T	GRCh38
NC_000023.10:g.66931441C>T , CM000685.1:g.66931441C>T	GRCh37
NC_000023.9:g.66848166C>T	NCBI36
NG_009014.2:g.172568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*431C>T	ENSP00000379358.4:n.*431C>T
ENST00000374690.9:c.2083C>T MANE Select	ENSP00000363822.3:p.Pro695Ser
ENST00000396043.3:c.710C>T	ENSP00000379358.3:n.710C>T
ENST00000396044.8:c.2083C>T	ENSP00000379359.3:p.Pro695Ser
ENST00000612452.5:c.2083C>T	ENSP00000484033.2:p.Pro695Ser
ENST00000374690.7:c.2083C>T	ENSP00000363822.3:p.Pro695Ser
ENST00000396043.2:c.487C>T	ENSP00000379358.2:p.Pro163Ser
ENST00000396044.7:c.2083C>T	ENSP00000379359.3:p.Pro695Ser
ENST00000612452.4:c.1513C>T	ENSP00000484033.1:p.Pro505Ser
NM_000044.3:c.2083C>T	NP_000035.2:p.Pro695Ser
NM_001011645.2:c.487C>T	NP_001011645.1:p.Pro163Ser
NM_000044.4:c.2083C>T	NP_000035.2:p.Pro695Ser
NM_001011645.3:c.487C>T	NP_001011645.1:p.Pro163Ser
NM_000044.6:c.2083C>T MANE Select	NP_000035.2:p.Pro695Ser