Canonical Allele Identifier: CA2573147341

Gene: MEN1

Linked Data

• ClinVar Variation Id: 1510884
• ClinVar RCV Id: RCV002043184
• dbSNP Id: rs2136130282

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64807098_64807099del , CM000673.2:g.64807098_64807099del	GRCh38
NC_000011.9:g.64574570_64574571del , CM000673.1:g.64574570_64574571del	GRCh37
NC_000011.8:g.64331146_64331147del	NCBI36
NG_008929.1:g.9196_9197del , LRG_509:g.9196_9197del
NG_033040.1:g.1143_1144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377313.7:c.840-1_840del
ENST00000394374.8:c.*133-1_*133del
ENST00000394376.7:c.825-1_825del
ENST00000413626.2:c.825-1_825del
ENST00000424912.2:c.825-1_825del
ENST00000429702.6:c.825-1_825del
ENST00000672079.2:c.825-1_825del
ENST00000710881.1:c.840-1_840del
ENST00000394374.7:c.572-1_572del
ENST00000394376.6:c.176-1_176del
ENST00000478548.3:n.857-1_857del
ENST00000671939.2:n.787-1_787del
ENST00000671965.2:n.564_565del
ENST00000312049.11:c.825-1_825del
ENST00000315422.9:c.825-1_825del
ENST00000377313.6:c.840-1_840del
ENST00000440873.6:c.825-1_825del
ENST00000450708.7:c.825-1_825del
ENST00000478548.2:n.865-1_865del
ENST00000671939.1:n.1102-1_1102del
ENST00000671965.1:n.564_565del
ENST00000672079.1:c.551-1_551del
ENST00000672304.1:c.825-1_825del
ENST00000312049.10:c.825-1_825del
ENST00000315422.8:c.825-1_825del
ENST00000337652.5:c.840-1_840del
ENST00000377313.5:c.840-1_840del
ENST00000377316.6:c.825-1_825del
ENST00000377321.5:c.720-1_720del
ENST00000377326.7:c.825-1_825del
ENST00000394374.6:c.840-1_840del
ENST00000394376.5:c.840-1_840del
ENST00000440873.5:c.825-1_825del
ENST00000450708.5:c.825-1_825del
NM_000244.3:c.840-1_840del , LRG_509t1:c.840-1_840del
NM_130799.2:c.825-1_825del , LRG_509t2:c.825-1_825del
NM_130800.2:c.840-1_840del
NM_130801.2:c.840-1_840del
NM_130802.2:c.840-1_840del
NM_130803.2:c.840-1_840del
NM_130804.2:c.840-1_840del
XM_005274001.3:c.825-1_825del
XM_011545040.1:c.825-1_825del
XM_011545041.1:c.825-1_825del
XM_011545042.1:c.825-1_825del
XM_005274001.4:c.825-1_825del
XM_011545041.2:c.825-1_825del
XM_011545042.3:c.825-1_825del
XM_017017765.1:c.840-1_840del
XM_017017766.1:c.840-1_840del
XM_017017767.2:c.840-1_840del
XM_017017768.1:c.840-1_840del
XM_017017769.1:c.825-1_825del
XM_017017770.2:c.825-1_825del
NM_001370251.1:c.825-1_825del
NM_001370259.2:c.825-1_825del
NM_001370260.1:c.825-1_825del
NM_001370261.1:c.825-1_825del
NM_001370262.1:c.720-1_720del
NM_001370263.1:c.720-1_720del
NM_000244.4:c.840-1_840del
NM_001370251.2:c.825-1_825del
NM_001370260.2:c.825-1_825del
NM_001370261.2:c.825-1_825del
NM_001370262.2:c.720-1_720del
NM_001370263.2:c.720-1_720del
NM_130799.3:c.825-1_825del
NM_130800.3:c.840-1_840del
NM_130801.3:c.840-1_840del
NM_130802.3:c.840-1_840del
NM_130803.3:c.840-1_840del
NM_130804.3:c.840-1_840del