Canonical Allele Identifier: CA10436421

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67546514_67546516del , CM000685.2:g.67546514_67546516del	GRCh38
NC_000023.10:g.66766356_66766358del , CM000685.1:g.66766356_66766358del	GRCh37
NC_000023.9:g.66683081_66683083del	NCBI36
NG_009014.2:g.7483_7485del

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.1368_1370del MANE Select	NP_000035.2:p.Gly457del
ENST00000374690.9:c.1368_1370del MANE Select	ENSP00000363822.3:p.Gly457del
NM_000044.3:c.1368_1370del	NP_000035.2:p.Gly457del
NM_000044.4:c.1368_1370del	NP_000035.2:p.Gly457del
NM_001011645.3:c.-416_-414del	NP_001011645.1:n.-416_-414del
NM_001348061.1:c.1368_1370del	NP_001334990.1:p.Gly457del
NM_001348063.1:c.1368_1370del	NP_001334992.1:p.Gly457del
NM_001348064.1:c.1368_1370del	NP_001334993.1:p.Gly457del
ENST00000374690.7:c.1368_1370del	ENSP00000363822.3:p.Gly457del
ENST00000396043.4:c.1368_1370del	ENSP00000379358.4:p.Gly457del
ENST00000396044.7:c.1368_1370del	ENSP00000379359.3:p.Gly457del
ENST00000396044.8:c.1368_1370del	ENSP00000379359.3:p.Gly457del
ENST00000504326.5:c.1368_1370del	ENSP00000421155.1:p.Gly457del
ENST00000513847.5:n.1695_1697del
ENST00000514029.5:c.1368_1370del	ENSP00000425199.1:p.Gly457del
ENST00000612010.4:c.1368_1370del	ENSP00000482407.1:p.Gly457del
ENST00000612452.4:c.798_800del	ENSP00000484033.1:p.Gly267del
ENST00000612452.5:c.1368_1370del	ENSP00000484033.2:p.Gly457del
ENST00000613054.2:c.1368_1370del	ENSP00000479013.1:p.Gly457del