Canonical Allele Identifier: CA516973458

Gene: AR

Linked Data

• gnomAD v4: X-67686044-T-C
• MyVariant Identifiers: chrX:g.66905886T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686044T>C , CM000685.2:g.67686044T>C	GRCh38
NC_000023.10:g.66905886T>C , CM000685.1:g.66905886T>C	GRCh37
NC_000023.9:g.66822611T>C	NCBI36
NG_009014.2:g.147013T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*151T>C	ENSP00000379358.4:n.*151T>C
ENST00000374690.9:c.1803T>C MANE Select	ENSP00000363822.3:p.Asp601=
ENST00000396043.3:c.430T>C	ENSP00000379358.3:n.430T>C
ENST00000396044.8:c.1803T>C	ENSP00000379359.3:p.Asp601=
ENST00000612452.5:c.1803T>C	ENSP00000484033.2:p.Asp601=
ENST00000374690.7:c.1803T>C	ENSP00000363822.3:p.Asp601=
ENST00000396043.2:c.207T>C	ENSP00000379358.2:p.Asp69=
ENST00000396044.7:c.1803T>C	ENSP00000379359.3:p.Asp601=
ENST00000504326.5:c.1803T>C	ENSP00000421155.1:p.Asp601=
ENST00000513847.5:n.2130T>C
ENST00000514029.5:c.*284T>C	ENSP00000425199.1:n.*284T>C
ENST00000612010.4:c.*155T>C	ENSP00000482407.1:n.*155T>C
ENST00000612452.4:c.1233T>C	ENSP00000484033.1:p.Asp411=
ENST00000613054.2:c.*1T>C	ENSP00000479013.1:n.*1T>C
NM_000044.3:c.1803T>C	NP_000035.2:p.Asp601=
NM_001011645.2:c.207T>C	NP_001011645.1:p.Asp69=
NM_000044.4:c.1803T>C	NP_000035.2:p.Asp601=
NM_001011645.3:c.207T>C	NP_001011645.1:p.Asp69=
NM_001348061.1:c.1803T>C	NP_001334990.1:p.Asp601=
NM_001348063.1:c.1803T>C	NP_001334992.1:p.Asp601=
NM_001348064.1:c.*1T>C	NP_001334993.1:n.*1T>C
NM_000044.6:c.1803T>C MANE Select	NP_000035.2:p.Asp601=