Canonical Allele Identifier: CA2693950285

Gene: AR

Linked Data

• gnomAD v4: X-67721702-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721704del , CM000685.2:g.67721704del	GRCh38
NC_000023.10:g.66941546del , CM000685.1:g.66941546del	GRCh37
NC_000023.9:g.66858271del	NCBI36
NG_009014.2:g.182673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667-129del	ENSP00000379358.4:n.*667-129del
ENST00000374690.9:c.2319-129del MANE Select	ENSP00000363822.3:n.2319-129del
ENST00000396043.3:c.946-129del	ENSP00000379358.3:n.946-129del
ENST00000396044.8:c.2174-1982del	ENSP00000379359.3:n.2174-1982del
ENST00000612452.5:c.2319-129del	ENSP00000484033.2:n.2319-129del
ENST00000374690.7:c.2319-129del	ENSP00000363822.3:n.2319-129del
ENST00000396043.2:c.723-129del	ENSP00000379358.2:n.723-129del
ENST00000396044.7:c.2174-1982del	ENSP00000379359.3:n.2174-1982del
ENST00000612452.4:c.1749-129del	ENSP00000484033.1:n.1749-129del
NM_000044.3:c.2319-129del	NP_000035.2:n.2319-129del
NM_001011645.2:c.723-129del	NP_001011645.1:n.723-129del
NM_000044.4:c.2319-129del	NP_000035.2:n.2319-129del
NM_001011645.3:c.723-129del	NP_001011645.1:n.723-129del
NM_000044.6:c.2319-129del MANE Select	NP_000035.2:n.2319-129del