Canonical Allele Identifier: CA413422893

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66863231T>G (hg19) ; chrX:g.67643389T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643389T>G , CM000685.2:g.67643389T>G	GRCh38
NC_000023.10:g.66863231T>G , CM000685.1:g.66863231T>G	GRCh37
NC_000023.9:g.66779956T>G	NCBI36
NG_009014.2:g.104358T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*98T>G	ENSP00000379358.4:n.*98T>G
ENST00000374690.9:c.1750T>G MANE Select	ENSP00000363822.3:p.Phe584Val
ENST00000396043.3:c.377T>G	ENSP00000379358.3:n.377T>G
ENST00000396044.8:c.1750T>G	ENSP00000379359.3:p.Phe584Val
ENST00000612452.5:c.1750T>G	ENSP00000484033.2:p.Phe584Val
ENST00000374690.7:c.1750T>G	ENSP00000363822.3:p.Phe584Val
ENST00000396043.2:c.154T>G	ENSP00000379358.2:p.Phe52Val
ENST00000396044.7:c.1750T>G	ENSP00000379359.3:p.Phe584Val
ENST00000504326.5:c.1750T>G	ENSP00000421155.1:p.Phe584Val
ENST00000513847.5:n.2077T>G
ENST00000514029.5:c.1750T>G	ENSP00000425199.1:p.Phe584Val
ENST00000612010.4:c.1750T>G	ENSP00000482407.1:p.Phe584Val
ENST00000612452.4:c.1180T>G	ENSP00000484033.1:p.Phe394Val
ENST00000613054.2:c.1617-42552T>G	ENSP00000479013.1:n.1617-42552T>G
NM_000044.3:c.1750T>G	NP_000035.2:p.Phe584Val
NM_001011645.2:c.154T>G	NP_001011645.1:p.Phe52Val
NM_000044.4:c.1750T>G	NP_000035.2:p.Phe584Val
NM_001011645.3:c.154T>G	NP_001011645.1:p.Phe52Val
NM_001348061.1:c.1750T>G	NP_001334990.1:p.Phe584Val
NM_001348063.1:c.1750T>G	NP_001334992.1:p.Phe584Val
NM_001348064.1:c.1617-42552T>G	NP_001334993.1:n.1617-42552T>G
NM_000044.6:c.1750T>G MANE Select	NP_000035.2:p.Phe584Val