Canonical Allele Identifier: CA2526936646
Gene: AR HGNC NCBI

Linked Data

gnomAD v4: X-67721805-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721810del , CM000685.2:g.67721810del GRCh38
NC_000023.10:g.66941652del , CM000685.1:g.66941652del GRCh37
NC_000023.9:g.66858377del NCBI36
NG_009014.2:g.182779del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*667-23del ENSP00000379358.4:n.*667-23del
ENST00000374690.9:c.2319-23del MANE Select ENSP00000363822.3:n.2319-23del
ENST00000396043.3:c.946-23del ENSP00000379358.3:n.946-23del
ENST00000396044.8:c.2174-1876del ENSP00000379359.3:n.2174-1876del
ENST00000612452.5:c.2319-23del ENSP00000484033.2:n.2319-23del
ENST00000374690.7:c.2319-23del ENSP00000363822.3:n.2319-23del
ENST00000396043.2:c.723-23del ENSP00000379358.2:n.723-23del
ENST00000396044.7:c.2174-1876del ENSP00000379359.3:n.2174-1876del
ENST00000612452.4:c.1749-23del ENSP00000484033.1:n.1749-23del
NM_000044.3:c.2319-23del NP_000035.2:n.2319-23del
NM_001011645.2:c.723-23del NP_001011645.1:n.723-23del
NM_000044.4:c.2319-23del NP_000035.2:n.2319-23del
NM_001011645.3:c.723-23del NP_001011645.1:n.723-23del
NM_000044.6:c.2319-23del MANE Select NP_000035.2:n.2319-23del
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