Canonical Allele Identifier: CA877566062

Gene: AR

Linked Data

• dbSNP Id: rs1440904113
• gnomAD v3: X-67721750-A-AG
• gnomAD v4: X-67721750-A-AG
• MyVariant Identifiers: chrX:g.66941592_66941593insG (hg19) ; chrX:g.67721750_67721751insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721753dup , CM000685.2:g.67721753dup	GRCh38
NC_000023.10:g.66941595dup , CM000685.1:g.66941595dup	GRCh37
NC_000023.9:g.66858320dup	NCBI36
NG_009014.2:g.182722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*667-80dup	ENSP00000379358.4:n.*667-80dup
ENST00000374690.9:c.2319-80dup MANE Select	ENSP00000363822.3:n.2319-80dup
ENST00000396043.3:c.946-80dup	ENSP00000379358.3:n.946-80dup
ENST00000396044.8:c.2174-1933dup	ENSP00000379359.3:n.2174-1933dup
ENST00000612452.5:c.2319-80dup	ENSP00000484033.2:n.2319-80dup
ENST00000374690.7:c.2319-80dup	ENSP00000363822.3:n.2319-80dup
ENST00000396043.2:c.723-80dup	ENSP00000379358.2:n.723-80dup
ENST00000396044.7:c.2174-1933dup	ENSP00000379359.3:n.2174-1933dup
ENST00000612452.4:c.1749-80dup	ENSP00000484033.1:n.1749-80dup
NM_000044.3:c.2319-80dup	NP_000035.2:n.2319-80dup
NM_001011645.2:c.723-80dup	NP_001011645.1:n.723-80dup
NM_000044.4:c.2319-80dup	NP_000035.2:n.2319-80dup
NM_001011645.3:c.723-80dup	NP_001011645.1:n.723-80dup
NM_000044.6:c.2319-80dup MANE Select	NP_000035.2:n.2319-80dup