Canonical Allele Identifier: CA2693923781

Gene: AR

Linked Data

• gnomAD v4: X-67544851-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67544851T>A , CM000685.2:g.67544851T>A	GRCh38
NC_000023.10:g.66764693T>A , CM000685.1:g.66764693T>A	GRCh37
NC_000023.9:g.66681418T>A	NCBI36
NG_009014.2:g.5820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-296T>A	ENSP00000379358.4:n.-296T>A
ENST00000374690.9:c.-296T>A MANE Select	ENSP00000363822.3:n.-296T>A
ENST00000612452.5:c.-296T>A	ENSP00000484033.2:n.-296T>A
ENST00000374690.7:c.-296T>A	ENSP00000363822.3:n.-296T>A
ENST00000396044.7:c.-296T>A	ENSP00000379359.3:n.-296T>A
ENST00000504326.5:c.-296T>A	ENSP00000421155.1:n.-296T>A
ENST00000513847.5:n.32T>A
ENST00000514029.5:c.-296T>A	ENSP00000425199.1:n.-296T>A
ENST00000612010.4:c.-296T>A	ENSP00000482407.1:n.-296T>A
ENST00000612452.4:c.-866T>A	ENSP00000484033.1:n.-866T>A
ENST00000613054.2:c.-296T>A	ENSP00000479013.1:n.-296T>A
NM_000044.3:c.-296T>A	NP_000035.2:n.-296T>A
NM_000044.4:c.-296T>A	NP_000035.2:n.-296T>A
NM_001011645.3:c.-2079T>A	NP_001011645.1:n.-2079T>A
NM_001348061.1:c.-296T>A	NP_001334990.1:n.-296T>A
NM_001348063.1:c.-296T>A	NP_001334992.1:n.-296T>A
NM_001348064.1:c.-296T>A	NP_001334993.1:n.-296T>A
NM_000044.6:c.-296T>A MANE Select	NP_000035.2:n.-296T>A