Canonical Allele Identifier: CA2695234347

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686067_67686071del , CM000685.2:g.67686067_67686071del	GRCh38
NC_000023.10:g.66905909_66905913del , CM000685.1:g.66905909_66905913del	GRCh37
NC_000023.9:g.66822634_66822638del	NCBI36
NG_009014.2:g.147036_147040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*174_*178del	ENSP00000379358.4:n.*174_*178del
ENST00000374690.9:c.1826_1830del MANE Select	ENSP00000363822.3:p.Arg609LysfsTer12
ENST00000396043.3:c.453_457del	ENSP00000379358.3:n.453_457del
ENST00000396044.8:c.1826_1830del	ENSP00000379359.3:p.Arg609LysfsTer12
ENST00000612452.5:c.1826_1830del	ENSP00000484033.2:p.Arg609LysfsTer12
ENST00000374690.7:c.1826_1830del	ENSP00000363822.3:p.Arg609LysfsTer12
ENST00000396043.2:c.230_234del	ENSP00000379358.2:p.Arg77LysfsTer12
ENST00000396044.7:c.1826_1830del	ENSP00000379359.3:p.Arg609LysfsTer12
ENST00000504326.5:c.1826_1830del	ENSP00000421155.1:p.Arg609LysfsTer12
ENST00000513847.5:n.2153_2157del
ENST00000514029.5:c.*307_*311del	ENSP00000425199.1:n.*307_*311del
ENST00000612010.4:c.*178_*182del	ENSP00000482407.1:n.*178_*182del
ENST00000612452.4:c.1256_1260del	ENSP00000484033.1:p.Arg419LysfsTer12
ENST00000613054.2:c.*24_*28del	ENSP00000479013.1:n.*24_*28del
NM_000044.3:c.1826_1830del	NP_000035.2:p.Arg609LysfsTer12
NM_001011645.2:c.230_234del	NP_001011645.1:p.Arg77LysfsTer12
NM_000044.4:c.1826_1830del	NP_000035.2:p.Arg609LysfsTer12
NM_001011645.3:c.230_234del	NP_001011645.1:p.Arg77LysfsTer12
NM_001348061.1:c.1826_1830del	NP_001334990.1:p.Arg609LysfsTer12
NM_001348063.1:c.1826_1830del	NP_001334992.1:p.Arg609LysfsTer12
NM_001348064.1:c.*24_*28del	NP_001334993.1:n.*24_*28del
NM_000044.6:c.1826_1830del MANE Select	NP_000035.2:p.Arg609LysfsTer12