Canonical Allele Identifier: CA413428198
Community Standard Title: NM_000044.6(AR):c.2631C>A (p.Phe877Leu)
Gene: AR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723709C>A , CM000685.2:g.67723709C>A GRCh38
NC_000023.10:g.66943551C>A , CM000685.1:g.66943551C>A GRCh37
NC_000023.9:g.66860276C>A NCBI36
NG_009014.2:g.184678C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2631C>A MANE Select NP_000035.2:p.Phe877Leu
ENST00000374690.9:c.2631C>A MANE Select ENSP00000363822.3:p.Phe877Leu
NM_000044.3:c.2631C>A NP_000035.2:p.Phe877Leu
NM_000044.4:c.2631C>A NP_000035.2:p.Phe877Leu
NM_001011645.2:c.1035C>A NP_001011645.1:p.Phe345Leu
NM_001011645.3:c.1035C>A NP_001011645.1:p.Phe345Leu
ENST00000374690.7:c.2631C>A ENSP00000363822.3:p.Phe877Leu
ENST00000396043.2:c.1035C>A ENSP00000379358.2:p.Phe345Leu
ENST00000396043.3:c.1258C>A ENSP00000379358.3:n.1258C>A
ENST00000396043.4:c.*979C>A ENSP00000379358.4:n.*979C>A
ENST00000396044.7:c.2197C>A ENSP00000379359.3:p.His733Asn
ENST00000396044.8:c.2197C>A ENSP00000379359.3:p.His733Asn
ENST00000612452.4:c.2082C>A ENSP00000484033.1:p.Phe694Leu
ENST00000612452.5:c.2631C>A ENSP00000484033.2:p.Phe877Leu
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