Canonical Allele Identifier: CA413422940

Gene: AR

Linked Data

• ClinVar Variation Id: 448902
• ClinVar RCV Id: RCV000517655 ; RCV000583701 ; RCV003151078
• dbSNP Id: rs1555982894
• MyVariant Identifiers: chrX:g.66863251T>C (hg19) ; chrX:g.67643409T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643409T>C , CM000685.2:g.67643409T>C	GRCh38
NC_000023.10:g.66863251T>C , CM000685.1:g.66863251T>C	GRCh37
NC_000023.9:g.66779976T>C	NCBI36
NG_009014.2:g.104378T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*116+2T>C	ENSP00000379358.4:n.*116+2T>C
ENST00000374690.9:c.1768+2T>C MANE Select	ENSP00000363822.3:n.1768+2T>C
ENST00000396043.3:c.395+2T>C	ENSP00000379358.3:n.395+2T>C
ENST00000396044.8:c.1768+2T>C	ENSP00000379359.3:n.1768+2T>C
ENST00000612452.5:c.1768+2T>C	ENSP00000484033.2:n.1768+2T>C
ENST00000374690.7:c.1768+2T>C	ENSP00000363822.3:n.1768+2T>C
ENST00000396043.2:c.172+2T>C	ENSP00000379358.2:n.172+2T>C
ENST00000396044.7:c.1768+2T>C	ENSP00000379359.3:n.1768+2T>C
ENST00000504326.5:c.1768+2T>C	ENSP00000421155.1:n.1768+2T>C
ENST00000513847.5:n.2095+2T>C
ENST00000514029.5:c.1768+2T>C	ENSP00000425199.1:n.1768+2T>C
ENST00000612010.4:c.1768+2T>C	ENSP00000482407.1:n.1768+2T>C
ENST00000612452.4:c.1198+2T>C	ENSP00000484033.1:n.1198+2T>C
ENST00000613054.2:c.1617-42532T>C	ENSP00000479013.1:n.1617-42532T>C
NM_000044.3:c.1768+2T>C	NP_000035.2:n.1768+2T>C
NM_001011645.2:c.172+2T>C	NP_001011645.1:n.172+2T>C
NM_000044.4:c.1768+2T>C	NP_000035.2:n.1768+2T>C
NM_001011645.3:c.172+2T>C	NP_001011645.1:n.172+2T>C
NM_001348061.1:c.1768+2T>C	NP_001334990.1:n.1768+2T>C
NM_001348063.1:c.1768+2T>C	NP_001334992.1:n.1768+2T>C
NM_001348064.1:c.1617-42532T>C	NP_001334993.1:n.1617-42532T>C
NM_000044.6:c.1768+2T>C MANE Select	NP_000035.2:n.1768+2T>C