Canonical Allele Identifier: CA10633145
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 366064
ClinVar RCV Id: RCV000267241
dbSNP Id: rs769884958

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.14735274del , CM000671.2:g.14735274del GRCh38
NC_000009.11:g.14735272del , CM000671.1:g.14735272del GRCh37
NC_000009.10:g.14725272del NCBI36
NG_017005.2:g.179966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000422223.6:c.*2125del ENSP00000412940.2:n.*2125del
NM_001177704.1:c.*2125del NP_001171175.1:n.*2125del
NM_144966.5:c.*2125del NP_659403.4:n.*2125del
XM_005251382.2:c.*2125del XP_005251439.1:n.*2125del
XM_005251384.3:c.*2125del XP_005251441.1:n.*2125del
XM_006716729.2:c.*2125del XP_006716792.1:n.*2125del
XM_011517748.1:c.*2125del XP_011516050.1:n.*2125del
XM_011517749.1:c.*2125del XP_011516051.1:n.*2125del
XM_011517750.1:c.*2125del XP_011516052.1:n.*2125del
XM_011517751.1:c.*2125del XP_011516053.1:n.*2125del
XM_011517752.1:c.*2125del XP_011516054.1:n.*2125del
XM_011517753.1:c.*2276del XP_011516055.1:n.*2276del
XM_011517758.1:c.*2125del XP_011516060.1:n.*2125del
XM_005251382.4:c.*2125del XP_005251439.1:n.*2125del
XM_005251384.4:c.*2125del XP_005251441.1:n.*2125del
XM_006716729.3:c.*2125del XP_006716792.1:n.*2125del
XM_011517758.2:c.*2125del XP_011516060.1:n.*2125del
XM_017014316.2:c.*2125del XP_016869805.1:n.*2125del
XM_017014317.1:c.*2125del XP_016869806.1:n.*2125del
XM_017014319.2:c.*2125del XP_016869808.1:n.*2125del
XM_017014320.2:c.*2125del XP_016869809.1:n.*2125del
XM_017014321.2:c.*2125del XP_016869810.1:n.*2125del
XM_017014322.1:c.*2125del XP_016869811.1:n.*2125del
XM_017014323.1:c.*2125del XP_016869812.1:n.*2125del
XM_017014324.2:c.*2125del XP_016869813.1:n.*2125del
XM_017014325.2:c.*2276del XP_016869814.1:n.*2276del
XM_017014326.1:c.*2125del XP_016869815.1:n.*2125del
XM_017014327.2:c.*2125del XP_016869816.1:n.*2125del
XR_001746194.2:n.9531del
XR_001746195.2:n.9528del
NM_001370058.1:c.*2276del NP_001356987.1:n.*2276del
NM_001370061.1:c.*2125del NP_001356990.1:n.*2125del
NR_163238.1:n.8055del
NR_163239.1:n.9473del
NR_163242.1:n.4487del