Canonical Allele Identifier: CA2695234386

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723732_67723733insCA , CM000685.2:g.67723732_67723733insCA	GRCh38
NC_000023.10:g.66943574_66943575insCA , CM000685.1:g.66943574_66943575insCA	GRCh37
NC_000023.9:g.66860299_66860300insCA	NCBI36
NG_009014.2:g.184701_184702insCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1002_*1003insCA	ENSP00000379358.4:n.*1002_*1003insCA
ENST00000374690.9:c.2654_2655insCA MANE Select	ENSP00000363822.3:p.His886AsnfsTer4
ENST00000396043.3:c.1281_1282insCA	ENSP00000379358.3:n.1281_1282insCA
ENST00000396044.8:c.*15_*16insCA	ENSP00000379359.3:n.*15_*16insCA
ENST00000612452.5:c.2654_2655insCA	ENSP00000484033.2:p.His886AsnfsTer4
ENST00000374690.7:c.2654_2655insCA	ENSP00000363822.3:p.His886AsnfsTer4
ENST00000396043.2:c.1058_1059insCA	ENSP00000379358.2:p.His354AsnfsTer4
ENST00000396044.7:c.*15_*16insCA	ENSP00000379359.3:n.*15_*16insCA
ENST00000612452.4:c.2105_2106insCA	ENSP00000484033.1:p.His703AsnfsTer4
NM_000044.3:c.2654_2655insCA	NP_000035.2:p.His886AsnfsTer4
NM_001011645.2:c.1058_1059insCA	NP_001011645.1:p.His354AsnfsTer4
NM_000044.4:c.2654_2655insCA	NP_000035.2:p.His886AsnfsTer4
NM_001011645.3:c.1058_1059insCA	NP_001011645.1:p.His354AsnfsTer4
NM_000044.6:c.2654_2655insCA MANE Select	NP_000035.2:p.His886AsnfsTer4