Canonical Allele Identifier: CA2695234371

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721892_67721893del , CM000685.2:g.67721892_67721893del	GRCh38
NC_000023.10:g.66941734_66941735del , CM000685.1:g.66941734_66941735del	GRCh37
NC_000023.9:g.66858459_66858460del	NCBI36
NG_009014.2:g.182861_182862del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*726_*727del	ENSP00000379358.4:n.*726_*727del
ENST00000374690.9:c.2378_2379del MANE Select	ENSP00000363822.3:p.Gln793ArgfsTer?
ENST00000396043.3:c.1005_1006del	ENSP00000379358.3:n.1005_1006del
ENST00000396044.8:c.2174-1794_2174-1793del	ENSP00000379359.3:n.2174-1794_2174-1793del
ENST00000612452.5:c.2378_2379del	ENSP00000484033.2:p.Gln793ArgfsTer?
ENST00000374690.7:c.2378_2379del	ENSP00000363822.3:p.Gln793ArgfsTer?
ENST00000396043.2:c.782_783del	ENSP00000379358.2:p.Gln261ArgfsTer?
ENST00000396044.7:c.2174-1794_2174-1793del	ENSP00000379359.3:n.2174-1794_2174-1793del
ENST00000612452.4:c.1808_1809del	ENSP00000484033.1:p.Gln603ArgfsTer24
NM_000044.3:c.2378_2379del	NP_000035.2:p.Gln793ArgfsTer?
NM_001011645.2:c.782_783del	NP_001011645.1:p.Gln261ArgfsTer?
NM_000044.4:c.2378_2379del	NP_000035.2:p.Gln793ArgfsTer?
NM_001011645.3:c.782_783del	NP_001011645.1:p.Gln261ArgfsTer?
NM_000044.6:c.2378_2379del MANE Select	NP_000035.2:p.Gln793ArgfsTer?