Canonical Allele Identifier: CA10436375

Gene: AR

Linked Data

• dbSNP Id: rs765067739
• ExAC: X:66766110 GCCGCCCCCT / G
• gnomAD v2: X-66766110-GCCGCCCCCT-G
• gnomAD v4: X-67546268-GCCGCCCCCT-G
• MyVariant Identifiers: chrX:g.66766111_66766119del (hg19) ; chrX:g.67546269_67546277del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67546274_67546282del , CM000685.2:g.67546274_67546282del	GRCh38
NC_000023.10:g.66766116_66766124del , CM000685.1:g.66766116_66766124del	GRCh37
NC_000023.9:g.66682841_66682849del	NCBI36
NG_009014.2:g.7243_7251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.1128_1136del	ENSP00000379358.4:p.Pro377_Pro379del
ENST00000374690.9:c.1128_1136del MANE Select	ENSP00000363822.3:p.Pro377_Pro379del
ENST00000396044.8:c.1128_1136del	ENSP00000379359.3:p.Pro377_Pro379del
ENST00000612452.5:c.1128_1136del	ENSP00000484033.2:p.Pro377_Pro379del
ENST00000374690.7:c.1128_1136del	ENSP00000363822.3:p.Pro377_Pro379del
ENST00000396044.7:c.1128_1136del	ENSP00000379359.3:p.Pro377_Pro379del
ENST00000504326.5:c.1128_1136del	ENSP00000421155.1:p.Pro377_Pro379del
ENST00000513847.5:n.1455_1463del
ENST00000514029.5:c.1128_1136del	ENSP00000425199.1:p.Pro377_Pro379del
ENST00000612010.4:c.1128_1136del	ENSP00000482407.1:p.Pro377_Pro379del
ENST00000612452.4:c.558_566del	ENSP00000484033.1:p.Pro187_Pro189del
ENST00000613054.2:c.1128_1136del	ENSP00000479013.1:p.Pro377_Pro379del
NM_000044.3:c.1128_1136del	NP_000035.2:p.Pro377_Pro379del
NM_000044.4:c.1128_1136del	NP_000035.2:p.Pro377_Pro379del
NM_001011645.3:c.-656_-648del	NP_001011645.1:n.-656_-648del
NM_001348061.1:c.1128_1136del	NP_001334990.1:p.Pro377_Pro379del
NM_001348063.1:c.1128_1136del	NP_001334992.1:p.Pro377_Pro379del
NM_001348064.1:c.1128_1136del	NP_001334993.1:p.Pro377_Pro379del
NM_000044.6:c.1128_1136del MANE Select	NP_000035.2:p.Pro377_Pro379del