Canonical Allele Identifier: CA413424176

Gene: AR

Linked Data

• ClinVar Variation Id: 458365
• ClinVar RCV Id: RCV001384434
• dbSNP Id: rs1555969545
• MyVariant Identifiers: chrX:g.66765256C>T (hg19) ; chrX:g.67545414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545414C>T , CM000685.2:g.67545414C>T	GRCh38
NC_000023.10:g.66765256C>T , CM000685.1:g.66765256C>T	GRCh37
NC_000023.9:g.66681981C>T	NCBI36
NG_009014.2:g.6383C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.268C>T	ENSP00000379358.4:p.Gln90Ter
ENST00000374690.9:c.268C>T MANE Select	ENSP00000363822.3:p.Gln90Ter
ENST00000396044.8:c.268C>T	ENSP00000379359.3:p.Gln90Ter
ENST00000612452.5:c.268C>T	ENSP00000484033.2:p.Gln90Ter
ENST00000374690.7:c.268C>T	ENSP00000363822.3:p.Gln90Ter
ENST00000396044.7:c.268C>T	ENSP00000379359.3:p.Gln90Ter
ENST00000504326.5:c.268C>T	ENSP00000421155.1:p.Gln90Ter
ENST00000513847.5:n.595C>T
ENST00000514029.5:c.268C>T	ENSP00000425199.1:p.Gln90Ter
ENST00000612010.4:c.268C>T	ENSP00000482407.1:p.Gln90Ter
ENST00000612452.4:c.-303C>T	ENSP00000484033.1:n.-303C>T
ENST00000613054.2:c.268C>T	ENSP00000479013.1:p.Gln90Ter
NM_000044.3:c.268C>T	NP_000035.2:p.Gln90Ter
NM_000044.4:c.268C>T	NP_000035.2:p.Gln90Ter
NM_001011645.3:c.-1516C>T	NP_001011645.1:n.-1516C>T
NM_001348061.1:c.268C>T	NP_001334990.1:p.Gln90Ter
NM_001348063.1:c.268C>T	NP_001334992.1:p.Gln90Ter
NM_001348064.1:c.268C>T	NP_001334993.1:p.Gln90Ter
NM_000044.6:c.268C>T MANE Select	NP_000035.2:p.Gln90Ter