Canonical Allele Identifier: CA330771842

Gene: AR

Linked Data

• dbSNP Id: rs969910786
• gnomAD v4: X-67717508-T-C
• MyVariant Identifiers: chrX:g.66937350T>C (hg19) ; chrX:g.67717508T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717508T>C , CM000685.2:g.67717508T>C	GRCh38
NC_000023.10:g.66937350T>C , CM000685.1:g.66937350T>C	GRCh37
NC_000023.9:g.66854075T>C	NCBI36
NG_009014.2:g.178477T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*552T>C	ENSP00000379358.4:n.*552T>C
ENST00000374690.9:c.2204T>C MANE Select	ENSP00000363822.3:p.Met735Thr
ENST00000396043.3:c.831T>C	ENSP00000379358.3:n.831T>C
ENST00000396044.8:c.2173+5819T>C	ENSP00000379359.3:n.2173+5819T>C
ENST00000612452.5:c.2204T>C	ENSP00000484033.2:p.Met735Thr
ENST00000374690.7:c.2204T>C	ENSP00000363822.3:p.Met735Thr
ENST00000396043.2:c.608T>C	ENSP00000379358.2:p.Met203Thr
ENST00000396044.7:c.2173+5819T>C	ENSP00000379359.3:n.2173+5819T>C
ENST00000612452.4:c.1634T>C	ENSP00000484033.1:p.Met545Thr
NM_000044.3:c.2204T>C	NP_000035.2:p.Met735Thr
NM_001011645.2:c.608T>C	NP_001011645.1:p.Met203Thr
NM_000044.4:c.2204T>C	NP_000035.2:p.Met735Thr
NM_001011645.3:c.608T>C	NP_001011645.1:p.Met203Thr
NM_000044.6:c.2204T>C MANE Select	NP_000035.2:p.Met735Thr