Canonical Allele Identifier: CA645554268
Gene: FREM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.14784635del , CM000671.2:g.14784635del GRCh38
NC_000009.11:g.14784633del , CM000671.1:g.14784633del GRCh37
NC_000009.10:g.14774633del NCBI36
NG_017005.2:g.130603del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380880.4:c.4178del
ENST00000380875.7:c.3981+8109del ENSP00000370257.3:n.3981+8109del
ENST00000380880.3:c.4178del
ENST00000422223.6:c.4178del
ENST00000466679.1:n.208del
ENST00000497634.2:n.339del
NM_144966.5:c.4178del
XM_005251382.2:c.4178del
XM_006716726.2:c.4178del
XM_011517748.1:c.4178del
XM_011517749.1:c.4178del
XM_011517750.1:c.4178del
XM_011517751.1:c.4178del
XM_011517752.1:c.4178del
XM_011517753.1:c.4178del
XM_011517754.1:c.4178del
XM_011517755.1:c.4178del
XM_011517756.1:c.4178del
XR_929188.1:n.4964del
XR_929190.1:n.5067del
XR_929487.1:n.89+4618del
XM_005251382.4:c.4178del
XM_005251384.4:c.-268del
XM_006716729.3:c.-265del
XM_017014316.2:c.4205del
XM_017014317.1:c.4205del
XM_017014319.2:c.4205del
XM_017014320.2:c.4205del
XM_017014321.2:c.4205del
XM_017014322.1:c.4205del
XM_017014323.1:c.4205del
XM_017014324.2:c.4205del
XM_017014325.2:c.4205del
XM_017014326.1:c.3797del
XM_017014327.2:c.3281del
XM_017014328.2:c.4205del
XM_017014329.2:c.4205del
XR_001746194.2:n.4991del
XR_001746195.2:n.4991del
XR_001746196.2:n.5094del
XR_001746197.2:n.4987del
NR_163238.1:n.4797+8109del
NR_163239.1:n.4933del
NM_001379081.2:c.4178del
NM_144966.7:c.4178del
NR_163238.2:n.4797+8109del
NR_163239.2:n.4933del