Canonical Allele Identifier: CA2509544522
Gene: LRPPRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43887164_43887165insAAAAAAAAAAAAAAGAAAAAAAAAAAAAA , CM000664.2:g.43887164_43887165insAAAAAAAAAAAAAAGAAAAAAAAAAAAAA GRCh38
NC_000002.11:g.44114303_44114304insAAAAAAAAAAAAAAGAAAAAAAAAAAAAA , CM000664.1:g.44114303_44114304insAAAAAAAAAAAAAAGAAAAAAAAAAAAAA GRCh37
NC_000002.10:g.43967807_43967808insAAAAAAAAAAAAAAGAAAAAAAAAAAAAA NCBI36
NG_008247.1:g.113855_113856insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682612.1:c.2401_2402insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000684454.1:n.9498_9499insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000260665.12:c.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000260665.7:n.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000260665.11:c.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000260665.7:n.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_133259.3:c.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_573566.2:n.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_002958896.1:n.5816_5817insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_133259.4:c.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_573566.2:n.*1449_*1450insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT