Canonical Allele Identifier: CA413429325

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66905940A>T (hg19) ; chrX:g.67686098A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686098A>T , CM000685.2:g.67686098A>T	GRCh38
NC_000023.10:g.66905940A>T , CM000685.1:g.66905940A>T	GRCh37
NC_000023.9:g.66822665A>T	NCBI36
NG_009014.2:g.147067A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*205A>T	ENSP00000379358.4:n.*205A>T
ENST00000374690.9:c.1857A>T MANE Select	ENSP00000363822.3:p.Lys619Asn
ENST00000396043.3:c.484A>T	ENSP00000379358.3:n.484A>T
ENST00000396044.8:c.1857A>T	ENSP00000379359.3:p.Lys619Asn
ENST00000612452.5:c.1857A>T	ENSP00000484033.2:p.Lys619Asn
ENST00000374690.7:c.1857A>T	ENSP00000363822.3:p.Lys619Asn
ENST00000396043.2:c.261A>T	ENSP00000379358.2:p.Lys87Asn
ENST00000396044.7:c.1857A>T	ENSP00000379359.3:p.Lys619Asn
ENST00000504326.5:c.1857A>T	ENSP00000421155.1:p.Lys619Asn
ENST00000513847.5:n.2184A>T
ENST00000514029.5:c.*338A>T	ENSP00000425199.1:n.*338A>T
ENST00000612010.4:c.*209A>T	ENSP00000482407.1:n.*209A>T
ENST00000612452.4:c.1287A>T	ENSP00000484033.1:p.Lys429Asn
ENST00000613054.2:c.*55A>T	ENSP00000479013.1:n.*55A>T
NM_000044.3:c.1857A>T	NP_000035.2:p.Lys619Asn
NM_001011645.2:c.261A>T	NP_001011645.1:p.Lys87Asn
NM_000044.4:c.1857A>T	NP_000035.2:p.Lys619Asn
NM_001011645.3:c.261A>T	NP_001011645.1:p.Lys87Asn
NM_001348061.1:c.1857A>T	NP_001334990.1:p.Lys619Asn
NM_001348063.1:c.1857A>T	NP_001334992.1:p.Lys619Asn
NM_001348064.1:c.*55A>T	NP_001334993.1:n.*55A>T
NM_000044.6:c.1857A>T MANE Select	NP_000035.2:p.Lys619Asn