Canonical Allele Identifier: CA2740092180

Gene: AR

Linked Data

• ClinVar Variation Id: 2947861
• ClinVar RCV Id: RCV003804491

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721820_67721822dup , CM000685.2:g.67721820_67721822dup	GRCh38
NC_000023.10:g.66941662_66941664dup , CM000685.1:g.66941662_66941664dup	GRCh37
NC_000023.9:g.66858387_66858389dup	NCBI36
NG_009014.2:g.182789_182791dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*667-13_*667-11dup	ENSP00000379358.4:n.*667-13_*667-11dup
ENST00000374690.9:c.2319-13_2319-11dup MANE Select	ENSP00000363822.3:n.2319-13_2319-11dup
ENST00000396043.3:c.946-13_946-11dup	ENSP00000379358.3:n.946-13_946-11dup
ENST00000396044.8:c.2174-1866_2174-1864dup	ENSP00000379359.3:n.2174-1866_2174-1864du...
ENST00000612452.5:c.2319-13_2319-11dup	ENSP00000484033.2:n.2319-13_2319-11dup
ENST00000374690.7:c.2319-13_2319-11dup	ENSP00000363822.3:n.2319-13_2319-11dup
ENST00000396043.2:c.723-13_723-11dup	ENSP00000379358.2:n.723-13_723-11dup
ENST00000396044.7:c.2174-1866_2174-1864dup	ENSP00000379359.3:n.2174-1866_2174-1864du...
ENST00000612452.4:c.1749-13_1749-11dup	ENSP00000484033.1:n.1749-13_1749-11dup
NM_000044.3:c.2319-13_2319-11dup	NP_000035.2:n.2319-13_2319-11dup
NM_001011645.2:c.723-13_723-11dup	NP_001011645.1:n.723-13_723-11dup
NM_000044.4:c.2319-13_2319-11dup	NP_000035.2:n.2319-13_2319-11dup
NM_001011645.3:c.723-13_723-11dup	NP_001011645.1:n.723-13_723-11dup
NM_000044.6:c.2319-13_2319-11dup MANE Select	NP_000035.2:n.2319-13_2319-11dup