Canonical Allele Identifier: CA10436505

Gene: AR

Linked Data

• ClinVar Variation Id: 2924024
• ClinVar RCV Id: RCV003785774
• dbSNP Id: rs756485947
• ExAC: X:66863242 C / T
• gnomAD v2: X-66863242-C-T
• gnomAD v3: X-67643400-C-T
• gnomAD v4: X-67643400-C-T
• COSMIC: COSM1124200
• MyVariant Identifiers: chrX:g.66863242C>T (hg19) ; chrX:g.67643400C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643400C>T , CM000685.2:g.67643400C>T	GRCh38
NC_000023.10:g.66863242C>T , CM000685.1:g.66863242C>T	GRCh37
NC_000023.9:g.66779967C>T	NCBI36
NG_009014.2:g.104369C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*109C>T	ENSP00000379358.4:n.*109C>T
ENST00000374690.9:c.1761C>T MANE Select	ENSP00000363822.3:p.Ala587=
ENST00000396043.3:c.388C>T	ENSP00000379358.3:n.388C>T
ENST00000396044.8:c.1761C>T	ENSP00000379359.3:p.Ala587=
ENST00000612452.5:c.1761C>T	ENSP00000484033.2:p.Ala587=
ENST00000374690.7:c.1761C>T	ENSP00000363822.3:p.Ala587=
ENST00000396043.2:c.165C>T	ENSP00000379358.2:p.Ala55=
ENST00000396044.7:c.1761C>T	ENSP00000379359.3:p.Ala587=
ENST00000504326.5:c.1761C>T	ENSP00000421155.1:p.Ala587=
ENST00000513847.5:n.2088C>T
ENST00000514029.5:c.1761C>T	ENSP00000425199.1:p.Ala587=
ENST00000612010.4:c.1761C>T	ENSP00000482407.1:p.Ala587=
ENST00000612452.4:c.1191C>T	ENSP00000484033.1:p.Ala397=
ENST00000613054.2:c.1617-42541C>T	ENSP00000479013.1:n.1617-42541C>T
NM_000044.3:c.1761C>T	NP_000035.2:p.Ala587=
NM_001011645.2:c.165C>T	NP_001011645.1:p.Ala55=
NM_000044.4:c.1761C>T	NP_000035.2:p.Ala587=
NM_001011645.3:c.165C>T	NP_001011645.1:p.Ala55=
NM_001348061.1:c.1761C>T	NP_001334990.1:p.Ala587=
NM_001348063.1:c.1761C>T	NP_001334992.1:p.Ala587=
NM_001348064.1:c.1617-42541C>T	NP_001334993.1:n.1617-42541C>T
NM_000044.6:c.1761C>T MANE Select	NP_000035.2:p.Ala587=