Canonical Allele Identifier: CA413424428

Gene: AR

Linked Data

• dbSNP Id: rs773708434
• COSMIC: COSM4136346 ; COSM4136347
• MyVariant Identifiers: chrX:g.66937352G>C (hg19) ; chrX:g.67717510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717510G>C , CM000685.2:g.67717510G>C	GRCh38
NC_000023.10:g.66937352G>C , CM000685.1:g.66937352G>C	GRCh37
NC_000023.9:g.66854077G>C	NCBI36
NG_009014.2:g.178479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*554G>C	ENSP00000379358.4:n.*554G>C
ENST00000374690.9:c.2206G>C MANE Select	ENSP00000363822.3:p.Ala736Pro
ENST00000396043.3:c.833G>C	ENSP00000379358.3:n.833G>C
ENST00000396044.8:c.2173+5821G>C	ENSP00000379359.3:n.2173+5821G>C
ENST00000612452.5:c.2206G>C	ENSP00000484033.2:p.Ala736Pro
ENST00000374690.7:c.2206G>C	ENSP00000363822.3:p.Ala736Pro
ENST00000396043.2:c.610G>C	ENSP00000379358.2:p.Ala204Pro
ENST00000396044.7:c.2173+5821G>C	ENSP00000379359.3:n.2173+5821G>C
ENST00000612452.4:c.1636G>C	ENSP00000484033.1:p.Ala546Pro
NM_000044.3:c.2206G>C	NP_000035.2:p.Ala736Pro
NM_001011645.2:c.610G>C	NP_001011645.1:p.Ala204Pro
NM_000044.4:c.2206G>C	NP_000035.2:p.Ala736Pro
NM_001011645.3:c.610G>C	NP_001011645.1:p.Ala204Pro
NM_000044.6:c.2206G>C MANE Select	NP_000035.2:p.Ala736Pro