Canonical Allele Identifier: CA2738703906

Gene: AR

Linked Data

• dbSNP Id: rs2147530626

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717491del , CM000685.2:g.67717491del	GRCh38
NC_000023.10:g.66937333del , CM000685.1:g.66937333del	GRCh37
NC_000023.9:g.66854058del	NCBI36
NG_009014.2:g.178460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*535del	ENSP00000379358.4:n.*535del
ENST00000374690.9:c.2187del MANE Select	ENSP00000363822.3:p.Leu729PhefsTer?
ENST00000396043.3:c.814del	ENSP00000379358.3:n.814del
ENST00000396044.8:c.2173+5802del	ENSP00000379359.3:n.2173+5802del
ENST00000612452.5:c.2187del	ENSP00000484033.2:p.Leu729PhefsTer?
ENST00000374690.7:c.2187del	ENSP00000363822.3:p.Leu729PhefsTer?
ENST00000396043.2:c.591del	ENSP00000379358.2:p.Leu197PhefsTer?
ENST00000396044.7:c.2173+5802del	ENSP00000379359.3:n.2173+5802del
ENST00000612452.4:c.1617del	ENSP00000484033.1:p.Leu539PhefsTer?
NM_000044.3:c.2187del	NP_000035.2:p.Leu729PhefsTer?
NM_001011645.2:c.591del	NP_001011645.1:p.Leu197PhefsTer?
NM_000044.4:c.2187del	NP_000035.2:p.Leu729PhefsTer?
NM_001011645.3:c.591del	NP_001011645.1:p.Leu197PhefsTer?
NM_000044.6:c.2187del MANE Select	NP_000035.2:p.Leu729PhefsTer?