Canonical Allele Identifier: CA2693950070

Gene: AR

Linked Data

• gnomAD v4: X-67711706-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711709del , CM000685.2:g.67711709del	GRCh38
NC_000023.10:g.66931551del , CM000685.1:g.66931551del	GRCh37
NC_000023.9:g.66848276del	NCBI36
NG_009014.2:g.172678del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*521+20del	ENSP00000379358.4:n.*521+20del
ENST00000374690.9:c.2173+20del MANE Select	ENSP00000363822.3:n.2173+20del
ENST00000396043.3:c.800+20del	ENSP00000379358.3:n.800+20del
ENST00000396044.8:c.2173+20del	ENSP00000379359.3:n.2173+20del
ENST00000612452.5:c.2173+20del	ENSP00000484033.2:n.2173+20del
ENST00000374690.7:c.2173+20del	ENSP00000363822.3:n.2173+20del
ENST00000396043.2:c.577+20del	ENSP00000379358.2:n.577+20del
ENST00000396044.7:c.2173+20del	ENSP00000379359.3:n.2173+20del
ENST00000612452.4:c.1603+20del	ENSP00000484033.1:n.1603+20del
NM_000044.3:c.2173+20del	NP_000035.2:n.2173+20del
NM_001011645.2:c.577+20del	NP_001011645.1:n.577+20del
NM_000044.4:c.2173+20del	NP_000035.2:n.2173+20del
NM_001011645.3:c.577+20del	NP_001011645.1:n.577+20del
NM_000044.6:c.2173+20del MANE Select	NP_000035.2:n.2173+20del