Canonical Allele Identifier: CA413429021

Gene: AR

Linked Data

• gnomAD v4: X-67685969-C-T
• MyVariant Identifiers: chrX:g.66905811C>T (hg19) ; chrX:g.67685969C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67685969C>T , CM000685.2:g.67685969C>T	GRCh38
NC_000023.10:g.66905811C>T , CM000685.1:g.66905811C>T	GRCh37
NC_000023.9:g.66822536C>T	NCBI36
NG_009014.2:g.146938C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*117-41C>T	ENSP00000379358.4:n.*117-41C>T
ENST00000374690.9:c.1769-41C>T MANE Select	ENSP00000363822.3:n.1769-41C>T
ENST00000396043.3:c.396-41C>T	ENSP00000379358.3:n.396-41C>T
ENST00000396044.8:c.1769-41C>T	ENSP00000379359.3:n.1769-41C>T
ENST00000612452.5:c.1769-41C>T	ENSP00000484033.2:n.1769-41C>T
ENST00000374690.7:c.1769-41C>T	ENSP00000363822.3:n.1769-41C>T
ENST00000396043.2:c.173-41C>T	ENSP00000379358.2:n.173-41C>T
ENST00000396044.7:c.1769-41C>T	ENSP00000379359.3:n.1769-41C>T
ENST00000504326.5:c.1769-41C>T	ENSP00000421155.1:n.1769-41C>T
ENST00000513847.5:n.2096-41C>T
ENST00000514029.5:c.*250-41C>T	ENSP00000425199.1:n.*250-41C>T
ENST00000612010.4:c.*121-41C>T	ENSP00000482407.1:n.*121-41C>T
ENST00000612452.4:c.1199-41C>T	ENSP00000484033.1:n.1199-41C>T
ENST00000613054.2:c.1645C>T	ENSP00000479013.1:p.Leu549Phe
NM_000044.3:c.1769-41C>T	NP_000035.2:n.1769-41C>T
NM_001011645.2:c.173-41C>T	NP_001011645.1:n.173-41C>T
NM_000044.4:c.1769-41C>T	NP_000035.2:n.1769-41C>T
NM_001011645.3:c.173-41C>T	NP_001011645.1:n.173-41C>T
NM_001348061.1:c.1769-41C>T	NP_001334990.1:n.1769-41C>T
NM_001348063.1:c.1769-41C>T	NP_001334992.1:n.1769-41C>T
NM_001348064.1:c.1645C>T	NP_001334993.1:p.Leu549Phe
NM_000044.6:c.1769-41C>T MANE Select	NP_000035.2:n.1769-41C>T