Canonical Allele Identifier: CA516970992

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66941789G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721947G>T , CM000685.2:g.67721947G>T	GRCh38
NC_000023.10:g.66941789G>T , CM000685.1:g.66941789G>T	GRCh37
NC_000023.9:g.66858514G>T	NCBI36
NG_009014.2:g.182916G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*781G>T	ENSP00000379358.4:n.*781G>T
ENST00000374690.9:c.2433G>T MANE Select	ENSP00000363822.3:p.Leu811=
ENST00000396043.3:c.1060G>T	ENSP00000379358.3:n.1060G>T
ENST00000396044.8:c.2174-1739G>T	ENSP00000379359.3:n.2174-1739G>T
ENST00000612452.5:c.2433G>T	ENSP00000484033.2:p.Leu811=
ENST00000374690.7:c.2433G>T	ENSP00000363822.3:p.Leu811=
ENST00000396043.2:c.837G>T	ENSP00000379358.2:p.Leu279=
ENST00000396044.7:c.2174-1739G>T	ENSP00000379359.3:n.2174-1739G>T
ENST00000612452.4:c.1863G>T	ENSP00000484033.1:p.Leu621=
NM_000044.3:c.2433G>T	NP_000035.2:p.Leu811=
NM_001011645.2:c.837G>T	NP_001011645.1:p.Leu279=
NM_000044.4:c.2433G>T	NP_000035.2:p.Leu811=
NM_001011645.3:c.837G>T	NP_001011645.1:p.Leu279=
NM_000044.6:c.2433G>T MANE Select	NP_000035.2:p.Leu811=