Canonical Allele Identifier: CA915948177
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 664768
ClinVar RCV Id: RCV000822934

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64805916_64807925del , CM000673.2:g.64805916_64807925del GRCh38
NC_000011.9:g.64573388_64575397del , CM000673.1:g.64573388_64575397del GRCh37
NC_000011.8:g.64329964_64331973del NCBI36
NG_008929.1:g.8373_10382del , LRG_509:g.8373_10382del
NG_033040.1:g.320_2329del

Transcript Alleles

HGVS Amino-acid change
ENST00000377313.7:c.638_1065-143del
ENST00000394374.8:c.623_*358-143del
ENST00000394376.7:c.623_1050-143del
ENST00000413626.2:c.623_1050-143del
ENST00000424912.2:c.623_1050-143del
ENST00000429702.6:c.623_1050-143del
ENST00000672079.2:c.623_*146-143del
ENST00000710881.1:c.638_1065-143del
ENST00000394374.7:c.384_797-143del
ENST00000478548.3:n.655_1400del
ENST00000671939.2:n.375_1012-143del
ENST00000671965.2:n.283_1432-143del
ENST00000312049.11:c.623_1050-143del
ENST00000315422.9:c.623_1050-143del
ENST00000377313.6:c.638_1065-143del
ENST00000440873.6:c.623_1050-143del
ENST00000450708.7:c.623_1050-143del
ENST00000478548.2:n.663_1408del
ENST00000671939.1:n.690_1327-143del
ENST00000672079.1:c.349_925-143del
ENST00000672304.1:c.623_1150del
ENST00000312049.10:c.623_1050-143del
ENST00000315422.8:c.623_1050-143del
ENST00000337652.5:c.638_1065-143del
ENST00000377313.5:c.638_1065-143del
ENST00000377316.6:c.623_1050-143del
ENST00000377321.5:c.549+74_945-143del
ENST00000377326.7:c.623_1050-143del
ENST00000394374.6:c.638_1065-143del
ENST00000394376.5:c.638_1065-143del
NM_000244.3:c.638_1065-143del , LRG_509t1:c.638_1065-143del
NM_130799.2:c.623_1050-143del , LRG_509t2:c.623_1050-143del
NM_130800.2:c.638_1065-143del
NM_130801.2:c.638_1065-143del
NM_130802.2:c.638_1065-143del
NM_130803.2:c.638_1065-143del
NM_130804.2:c.638_1065-143del
XM_005274001.3:c.623_1050-143del
XM_011545040.1:c.623_1150del
XM_011545041.1:c.623_1150del
XM_011545042.1:c.623_1150del
XM_005274001.4:c.623_1050-143del
XM_011545041.2:c.623_1150del
XM_011545042.3:c.623_1150del
XM_017017765.1:c.638_1165del
XM_017017766.1:c.638_1165del
XM_017017767.2:c.638_1165del
XM_017017768.1:c.638_1165del
XM_017017769.1:c.623_1050-143del
XM_017017770.2:c.623_1050-143del
NM_001370251.1:c.623_1150del
NM_001370259.2:c.623_1050-143del
NM_001370260.1:c.623_1050-143del
NM_001370261.1:c.623_1050-143del
NM_001370262.1:c.549+74_945-143del
NM_001370263.1:c.549+74_945-143del
NM_000244.4:c.638_1065-143del
NM_001370251.2:c.623_1150del
NM_001370260.2:c.623_1050-143del
NM_001370261.2:c.623_1050-143del
NM_001370262.2:c.549+74_945-143del
NM_001370263.2:c.549+74_945-143del
NM_130799.3:c.623_1050-143del
NM_130800.3:c.638_1065-143del
NM_130801.3:c.638_1065-143del
NM_130802.3:c.638_1065-143del
NM_130803.3:c.638_1065-143del
NM_130804.3:c.638_1065-143del