Canonical Allele Identifier: CA917323542
Gene: FREM3 HGNC NCBI
GUSBP5 HGNC NCBI

Linked Data

dbSNP Id: rs1578821952

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.143587658dup , CM000666.2:g.143587658dup GRCh38
NC_000004.11:g.144508811dup , CM000666.1:g.144508811dup GRCh37
NC_000004.10:g.144728261dup NCBI36
NG_052820.1:g.118019dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000329798.5:c.6029-1664dup (FREM3) MANE Select ENSP00000332886.5:n.6029-1664dup
ENST00000511042.5:n.191+15077dup (GUSBP5)
NM_001168235.1:c.6029-1664dup (FREM3) NP_001161707.1:n.6029-1664dup
NM_001168235.2:c.6029-1664dup (FREM3) MANE Select NP_001161707.1:n.6029-1664dup