Canonical Allele Identifier: CA915951140

Gene: AR

Linked Data

• ClinVar Variation Id: 649268
• ClinVar RCV Id: RCV000804161
• dbSNP Id: rs1602279488

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722923dup , CM000685.2:g.67722923dup	GRCh38
NC_000023.10:g.66942765dup , CM000685.1:g.66942765dup	GRCh37
NC_000023.9:g.66859490dup	NCBI36
NG_009014.2:g.183892dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*894dup	ENSP00000379358.4:n.*894dup
ENST00000374690.9:c.2546dup MANE Select	ENSP00000363822.3:p.Asn849LysfsTer?
ENST00000396043.3:c.1173dup	ENSP00000379358.3:n.1173dup
ENST00000396044.8:c.2174-763dup	ENSP00000379359.3:n.2174-763dup
ENST00000612452.5:c.2546dup	ENSP00000484033.2:p.Asn849LysfsTer?
ENST00000374690.7:c.2546dup	ENSP00000363822.3:p.Asn849LysfsTer?
ENST00000396043.2:c.950dup	ENSP00000379358.2:p.Asn317LysfsTer?
ENST00000396044.7:c.2174-763dup	ENSP00000379359.3:n.2174-763dup
ENST00000612452.4:c.1997dup	ENSP00000484033.1:p.Asn666LysfsTer?
NM_000044.3:c.2546dup	NP_000035.2:p.Asn849LysfsTer?
NM_001011645.2:c.950dup	NP_001011645.1:p.Asn317LysfsTer?
NM_000044.4:c.2546dup	NP_000035.2:p.Asn849LysfsTer?
NM_001011645.3:c.950dup	NP_001011645.1:p.Asn317LysfsTer?
NM_000044.6:c.2546dup MANE Select	NP_000035.2:p.Asn849LysfsTer?