Canonical Allele Identifier: CA2548932409

Gene: AR

Linked Data

• ClinVar Variation Id: 2928888
• ClinVar RCV Id: RCV003781614
• gnomAD v4: X-67722808-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722808T>C , CM000685.2:g.67722808T>C	GRCh38
NC_000023.10:g.66942650T>C , CM000685.1:g.66942650T>C	GRCh37
NC_000023.9:g.66859375T>C	NCBI36
NG_009014.2:g.183777T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*798-19T>C	ENSP00000379358.4:n.*798-19T>C
ENST00000374690.9:c.2450-19T>C MANE Select	ENSP00000363822.3:n.2450-19T>C
ENST00000396043.3:c.1077-19T>C	ENSP00000379358.3:n.1077-19T>C
ENST00000396044.8:c.2174-878T>C	ENSP00000379359.3:n.2174-878T>C
ENST00000612452.5:c.2450-19T>C	ENSP00000484033.2:n.2450-19T>C
ENST00000374690.7:c.2450-19T>C	ENSP00000363822.3:n.2450-19T>C
ENST00000396043.2:c.854-19T>C	ENSP00000379358.2:n.854-19T>C
ENST00000396044.7:c.2174-878T>C	ENSP00000379359.3:n.2174-878T>C
ENST00000612452.4:c.1901-19T>C	ENSP00000484033.1:n.1901-19T>C
NM_000044.3:c.2450-19T>C	NP_000035.2:n.2450-19T>C
NM_001011645.2:c.854-19T>C	NP_001011645.1:n.854-19T>C
NM_000044.4:c.2450-19T>C	NP_000035.2:n.2450-19T>C
NM_001011645.3:c.854-19T>C	NP_001011645.1:n.854-19T>C
NM_000044.6:c.2450-19T>C MANE Select	NP_000035.2:n.2450-19T>C