Canonical Allele Identifier: CA10436546

Gene: AR

Linked Data

• dbSNP Id: rs752446184
• ExAC: X:66931207 C / CTGA
• gnomAD v2: X-66931207-C-CTGA
• gnomAD v3: X-67711365-C-CTGA
• gnomAD v4: X-67711365-C-CTGA
• MyVariant Identifiers: chrX:g.66931207_66931208insTGA (hg19) ; chrX:g.67711365_67711366insTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711370_67711372dup , CM000685.2:g.67711370_67711372dup	GRCh38
NC_000023.10:g.66931212_66931214dup , CM000685.1:g.66931212_66931214dup	GRCh37
NC_000023.9:g.66847937_66847939dup	NCBI36
NG_009014.2:g.172339_172341dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*234-32_*234-30dup	ENSP00000379358.4:n.*234-32_*234-30dup
ENST00000374690.9:c.1886-32_1886-30dup MANE Select	ENSP00000363822.3:n.1886-32_1886-30dup
ENST00000396043.3:c.513-32_513-30dup	ENSP00000379358.3:n.513-32_513-30dup
ENST00000396044.8:c.1886-32_1886-30dup	ENSP00000379359.3:n.1886-32_1886-30dup
ENST00000612452.5:c.1886-32_1886-30dup	ENSP00000484033.2:n.1886-32_1886-30dup
ENST00000374690.7:c.1886-32_1886-30dup	ENSP00000363822.3:n.1886-32_1886-30dup
ENST00000396043.2:c.290-32_290-30dup	ENSP00000379358.2:n.290-32_290-30dup
ENST00000396044.7:c.1886-32_1886-30dup	ENSP00000379359.3:n.1886-32_1886-30dup
ENST00000612452.4:c.1316-32_1316-30dup	ENSP00000484033.1:n.1316-32_1316-30dup
NM_000044.3:c.1886-32_1886-30dup	NP_000035.2:n.1886-32_1886-30dup
NM_001011645.2:c.290-32_290-30dup	NP_001011645.1:n.290-32_290-30dup
NM_000044.4:c.1886-32_1886-30dup	NP_000035.2:n.1886-32_1886-30dup
NM_001011645.3:c.290-32_290-30dup	NP_001011645.1:n.290-32_290-30dup
NM_000044.6:c.1886-32_1886-30dup MANE Select	NP_000035.2:n.1886-32_1886-30dup