Canonical Allele Identifier: CA413426624

Gene: AR

Linked Data

• dbSNP Id: rs1254203917
• gnomAD v2: X-66941723-G-T
• MyVariant Identifiers: chrX:g.66941723G>T (hg19) ; chrX:g.67721881G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721881G>T , CM000685.2:g.67721881G>T	GRCh38
NC_000023.10:g.66941723G>T , CM000685.1:g.66941723G>T	GRCh37
NC_000023.9:g.66858448G>T	NCBI36
NG_009014.2:g.182850G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*715G>T	ENSP00000379358.4:n.*715G>T
ENST00000374690.9:c.2367G>T MANE Select	ENSP00000363822.3:p.Arg789Ser
ENST00000396043.3:c.994G>T	ENSP00000379358.3:n.994G>T
ENST00000396044.8:c.2174-1805G>T	ENSP00000379359.3:n.2174-1805G>T
ENST00000612452.5:c.2367G>T	ENSP00000484033.2:p.Arg789Ser
ENST00000374690.7:c.2367G>T	ENSP00000363822.3:p.Arg789Ser
ENST00000396043.2:c.771G>T	ENSP00000379358.2:p.Arg257Ser
ENST00000396044.7:c.2174-1805G>T	ENSP00000379359.3:n.2174-1805G>T
ENST00000612452.4:c.1797G>T	ENSP00000484033.1:p.Arg599Ser
NM_000044.3:c.2367G>T	NP_000035.2:p.Arg789Ser
NM_001011645.2:c.771G>T	NP_001011645.1:p.Arg257Ser
NM_000044.4:c.2367G>T	NP_000035.2:p.Arg789Ser
NM_001011645.3:c.771G>T	NP_001011645.1:p.Arg257Ser
NM_000044.6:c.2367G>T MANE Select	NP_000035.2:p.Arg789Ser