Canonical Allele Identifier: CA10436703

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723690C>T , CM000685.2:g.67723690C>T	GRCh38
NC_000023.10:g.66943532C>T , CM000685.1:g.66943532C>T	GRCh37
NC_000023.9:g.66860257C>T	NCBI36
NG_009014.2:g.184659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*960C>T	ENSP00000379358.4:n.*960C>T
ENST00000374690.9:c.2612C>T MANE Select	ENSP00000363822.3:p.Ala871Val
ENST00000396043.3:c.1239C>T	ENSP00000379358.3:n.1239C>T
ENST00000396044.8:c.2178C>T	ENSP00000379359.3:p.Cys726=
ENST00000612452.5:c.2612C>T	ENSP00000484033.2:p.Ala871Val
ENST00000374690.7:c.2612C>T	ENSP00000363822.3:p.Ala871Val
ENST00000396043.2:c.1016C>T	ENSP00000379358.2:p.Ala339Val
ENST00000396044.7:c.2178C>T	ENSP00000379359.3:p.Cys726=
ENST00000612452.4:c.2063C>T	ENSP00000484033.1:p.Ala688Val
NM_000044.3:c.2612C>T	NP_000035.2:p.Ala871Val
NM_001011645.2:c.1016C>T	NP_001011645.1:p.Ala339Val
NM_000044.4:c.2612C>T	NP_000035.2:p.Ala871Val
NM_001011645.3:c.1016C>T	NP_001011645.1:p.Ala339Val
NM_000044.6:c.2612C>T MANE Select	NP_000035.2:p.Ala871Val