Canonical Allele Identifier: CA359838569

Gene: IPO11 LRRC70

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.62580226G>C , CM000667.2:g.62580226G>C	GRCh38
NC_000005.9:g.61876053G>C , CM000667.1:g.61876053G>C	GRCh37
NC_000005.8:g.61911809G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016338.5:c.2583-11351G>C (IPO11) MANE Select	NP_057422.3:n.2583-11351G>C
NM_181506.5:c.788G>C (LRRC70) MANE Select	NP_852607.3:p.Arg263Thr
ENST00000325324.11:c.2583-11351G>C (IPO11) MANE Select	ENSP00000316651.6:n.2583-11351G>C
ENST00000334994.6:c.788G>C (LRRC70) MANE Select	ENSP00000399441.1:p.Arg263Thr
NM_001134779.1:c.2703-11351G>C (IPO11)	NP_001128251.1:n.2703-11351G>C
NM_001134779.2:c.2703-11351G>C (IPO11)	NP_001128251.1:n.2703-11351G>C
NM_016338.4:c.2583-11351G>C (IPO11)	NP_057422.3:n.2583-11351G>C
NM_181506.4:c.788G>C (LRRC70)	NP_852607.3:p.Arg263Thr
NR_073584.1:n.201+1291G>C
ENST00000325324.10:c.2583-11351G>C (IPO11)	ENSP00000316651.6:n.2583-11351G>C
ENST00000334994.5:c.788G>C (LRRC70)	ENSP00000399441.1:p.Arg263Thr
ENST00000409296.7:c.2703-11351G>C (IPO11)	ENSP00000386992.3:n.2703-11351G>C
ENST00000409534.1:c.-62+1291G>C (IPO11)	ENSP00000387039.1:n.-62+1291G>C
ENST00000413749.2:c.355-228G>C (IPO11)	ENSP00000398230.1:n.355-228G>C
ENST00000424533.5:c.*74-228G>C (IPO11)	ENSP00000395685.1:n.*74-228G>C
ENST00000448151.2:n.183-228G>C (LRRC70)
ENST00000491184.2:c.195-228G>C (LRRC70)	ENSP00000427117.1:n.195-228G>C
ENST00000511133.1:n.433-11351G>C (IPO11)
ENST00000511713.5:c.377-11351G>C (IPO11)