Canonical Allele Identifier: CA2740092181

Gene: AR

Linked Data

• ClinVar Variation Id: 2929766
• ClinVar RCV Id: RCV003784932

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721825C>T , CM000685.2:g.67721825C>T	GRCh38
NC_000023.10:g.66941667C>T , CM000685.1:g.66941667C>T	GRCh37
NC_000023.9:g.66858392C>T	NCBI36
NG_009014.2:g.182794C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*667-8C>T	ENSP00000379358.4:n.*667-8C>T
ENST00000374690.9:c.2319-8C>T MANE Select	ENSP00000363822.3:n.2319-8C>T
ENST00000396043.3:c.946-8C>T	ENSP00000379358.3:n.946-8C>T
ENST00000396044.8:c.2174-1861C>T	ENSP00000379359.3:n.2174-1861C>T
ENST00000612452.5:c.2319-8C>T	ENSP00000484033.2:n.2319-8C>T
ENST00000374690.7:c.2319-8C>T	ENSP00000363822.3:n.2319-8C>T
ENST00000396043.2:c.723-8C>T	ENSP00000379358.2:n.723-8C>T
ENST00000396044.7:c.2174-1861C>T	ENSP00000379359.3:n.2174-1861C>T
ENST00000612452.4:c.1749-8C>T	ENSP00000484033.1:n.1749-8C>T
NM_000044.3:c.2319-8C>T	NP_000035.2:n.2319-8C>T
NM_001011645.2:c.723-8C>T	NP_001011645.1:n.723-8C>T
NM_000044.4:c.2319-8C>T	NP_000035.2:n.2319-8C>T
NM_001011645.3:c.723-8C>T	NP_001011645.1:n.723-8C>T
NM_000044.6:c.2319-8C>T MANE Select	NP_000035.2:n.2319-8C>T