Canonical Allele Identifier: CA642369183

Gene: AR

Linked Data

• dbSNP Id: rs1240086021
• gnomAD v2: X-66764788-GTCT-G
• gnomAD v3: X-67544946-GTCT-G
• gnomAD v4: X-67544946-GTCT-G
• MyVariant Identifiers: chrX:g.66764789_66764791del (hg19) ; chrX:g.67544947_67544949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67544953_67544955del , CM000685.2:g.67544953_67544955del	GRCh38
NC_000023.10:g.66764795_66764797del , CM000685.1:g.66764795_66764797del	GRCh37
NC_000023.9:g.66681520_66681522del	NCBI36
NG_009014.2:g.5922_5924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-194_-192del	ENSP00000379358.4:n.-194_-192del
ENST00000374690.9:c.-194_-192del MANE Select	ENSP00000363822.3:n.-194_-192del
ENST00000612452.5:c.-194_-192del	ENSP00000484033.2:n.-194_-192del
ENST00000374690.7:c.-194_-192del	ENSP00000363822.3:n.-194_-192del
ENST00000396044.7:c.-194_-192del	ENSP00000379359.3:n.-194_-192del
ENST00000504326.5:c.-194_-192del	ENSP00000421155.1:n.-194_-192del
ENST00000513847.5:n.134_136del
ENST00000514029.5:c.-194_-192del	ENSP00000425199.1:n.-194_-192del
ENST00000612010.4:c.-194_-192del	ENSP00000482407.1:n.-194_-192del
ENST00000612452.4:c.-764_-762del	ENSP00000484033.1:n.-764_-762del
ENST00000613054.2:c.-194_-192del	ENSP00000479013.1:n.-194_-192del
NM_000044.3:c.-194_-192del	NP_000035.2:n.-194_-192del
NM_000044.4:c.-194_-192del	NP_000035.2:n.-194_-192del
NM_001011645.3:c.-1977_-1975del	NP_001011645.1:n.-1977_-1975del
NM_001348061.1:c.-194_-192del	NP_001334990.1:n.-194_-192del
NM_001348063.1:c.-194_-192del	NP_001334992.1:n.-194_-192del
NM_001348064.1:c.-194_-192del	NP_001334993.1:n.-194_-192del
NM_000044.6:c.-194_-192del MANE Select	NP_000035.2:n.-194_-192del