Canonical Allele Identifier: CA2693949602

Gene: AR

Linked Data

• gnomAD v4: X-67685839-CTGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67685842_67685845del , CM000685.2:g.67685842_67685845del	GRCh38
NC_000023.10:g.66905684_66905687del , CM000685.1:g.66905684_66905687del	GRCh37
NC_000023.9:g.66822409_66822412del	NCBI36
NG_009014.2:g.146811_146814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*117-168_*117-165del	ENSP00000379358.4:n.*117-168_*117-165del
ENST00000374690.9:c.1769-168_1769-165del MANE Select	ENSP00000363822.3:n.1769-168_1769-165del
ENST00000396043.3:c.396-168_396-165del	ENSP00000379358.3:n.396-168_396-165del
ENST00000396044.8:c.1769-168_1769-165del	ENSP00000379359.3:n.1769-168_1769-165del
ENST00000612452.5:c.1769-168_1769-165del	ENSP00000484033.2:n.1769-168_1769-165del
ENST00000374690.7:c.1769-168_1769-165del	ENSP00000363822.3:n.1769-168_1769-165del
ENST00000396043.2:c.173-168_173-165del	ENSP00000379358.2:n.173-168_173-165del
ENST00000396044.7:c.1769-168_1769-165del	ENSP00000379359.3:n.1769-168_1769-165del
ENST00000504326.5:c.1769-168_1769-165del	ENSP00000421155.1:n.1769-168_1769-165del
ENST00000513847.5:n.2096-168_2096-165del
ENST00000514029.5:c.*250-168_*250-165del	ENSP00000425199.1:n.*250-168_*250-165del
ENST00000612010.4:c.*121-168_*121-165del	ENSP00000482407.1:n.*121-168_*121-165del
ENST00000612452.4:c.1199-168_1199-165del	ENSP00000484033.1:n.1199-168_1199-165del
ENST00000613054.2:c.1617-99_1617-96del	ENSP00000479013.1:n.1617-99_1617-96del
NM_000044.3:c.1769-168_1769-165del	NP_000035.2:n.1769-168_1769-165del
NM_001011645.2:c.173-168_173-165del	NP_001011645.1:n.173-168_173-165del
NM_000044.4:c.1769-168_1769-165del	NP_000035.2:n.1769-168_1769-165del
NM_001011645.3:c.173-168_173-165del	NP_001011645.1:n.173-168_173-165del
NM_001348061.1:c.1769-168_1769-165del	NP_001334990.1:n.1769-168_1769-165del
NM_001348063.1:c.1769-168_1769-165del	NP_001334992.1:n.1769-168_1769-165del
NM_001348064.1:c.1617-99_1617-96del	NP_001334993.1:n.1617-99_1617-96del
NM_000044.6:c.1769-168_1769-165del MANE Select	NP_000035.2:n.1769-168_1769-165del