Canonical Allele Identifier: CA413422890

Gene: AR

Linked Data

• ClinVar Variation Id: 1805862
• ClinVar RCV Id: RCV002472280
• dbSNP Id: rs2147436658
• MyVariant Identifiers: chrX:g.66863230C>G (hg19) ; chrX:g.67643388C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643388C>G , CM000685.2:g.67643388C>G	GRCh38
NC_000023.10:g.66863230C>G , CM000685.1:g.66863230C>G	GRCh37
NC_000023.9:g.66779955C>G	NCBI36
NG_009014.2:g.104357C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*97C>G	ENSP00000379358.4:n.*97C>G
ENST00000374690.9:c.1749C>G MANE Select	ENSP00000363822.3:p.Phe583Leu
ENST00000396043.3:c.376C>G	ENSP00000379358.3:n.376C>G
ENST00000396044.8:c.1749C>G	ENSP00000379359.3:p.Phe583Leu
ENST00000612452.5:c.1749C>G	ENSP00000484033.2:p.Phe583Leu
ENST00000374690.7:c.1749C>G	ENSP00000363822.3:p.Phe583Leu
ENST00000396043.2:c.153C>G	ENSP00000379358.2:p.Phe51Leu
ENST00000396044.7:c.1749C>G	ENSP00000379359.3:p.Phe583Leu
ENST00000504326.5:c.1749C>G	ENSP00000421155.1:p.Phe583Leu
ENST00000513847.5:n.2076C>G
ENST00000514029.5:c.1749C>G	ENSP00000425199.1:p.Phe583Leu
ENST00000612010.4:c.1749C>G	ENSP00000482407.1:p.Phe583Leu
ENST00000612452.4:c.1179C>G	ENSP00000484033.1:p.Phe393Leu
ENST00000613054.2:c.1617-42553C>G	ENSP00000479013.1:n.1617-42553C>G
NM_000044.3:c.1749C>G	NP_000035.2:p.Phe583Leu
NM_001011645.2:c.153C>G	NP_001011645.1:p.Phe51Leu
NM_000044.4:c.1749C>G	NP_000035.2:p.Phe583Leu
NM_001011645.3:c.153C>G	NP_001011645.1:p.Phe51Leu
NM_001348061.1:c.1749C>G	NP_001334990.1:p.Phe583Leu
NM_001348063.1:c.1749C>G	NP_001334992.1:p.Phe583Leu
NM_001348064.1:c.1617-42553C>G	NP_001334993.1:n.1617-42553C>G
NM_000044.6:c.1749C>G MANE Select	NP_000035.2:p.Phe583Leu