Canonical Allele Identifier: CA915948180
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 827534
ClinVar RCV Id: RCV001027323
dbSNP Id: rs1592646831

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64807095_64807099delinsAACCTCTAGGTA , CM000673.2:g.64807095_64807099delinsAACCTCTAGGTA GRCh38
NC_000011.9:g.64574567_64574571delinsAACCTCTAGGTA , CM000673.1:g.64574567_64574571delinsAACCTCTAGGTA GRCh37
NC_000011.8:g.64331143_64331147delinsAACCTCTAGGTA NCBI36
NG_008929.1:g.9196_9200delinsTACCTAGAGGTT , LRG_509:g.9196_9200delinsTACCTAGAGGTT
NG_033040.1:g.1143_1147delinsTACCTAGAGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000377313.7:c.840-1_843delinsTACCTAGAGGTT
ENST00000394374.8:c.*133-1_*136delinsTACCTAGAGGTT
ENST00000394376.7:c.825-1_828delinsTACCTAGAGGTT
ENST00000413626.2:c.825-1_828delinsTACCTAGAGGTT
ENST00000424912.2:c.825-1_828delinsTACCTAGAGGTT
ENST00000429702.6:c.825-1_828delinsTACCTAGAGGTT
ENST00000672079.2:c.825-1_828delinsTACCTAGAGGTT
ENST00000710881.1:c.840-1_843delinsTACCTAGAGGTT
ENST00000394374.7:c.572-1_575delinsTACCTAGAGGTT
ENST00000394376.6:c.176-1_179delinsTACCTAGAGGTT
ENST00000478548.3:n.857-1_860delinsTACCTAGAGGTT
ENST00000671939.2:n.787-1_790delinsTACCTAGAGGTT
ENST00000671965.2:n.564_568delinsTACCTAGAGGTT
ENST00000312049.11:c.825-1_828delinsTACCTAGAGGTT
ENST00000315422.9:c.825-1_828delinsTACCTAGAGGTT
ENST00000377313.6:c.840-1_843delinsTACCTAGAGGTT
ENST00000440873.6:c.825-1_828delinsTACCTAGAGGTT
ENST00000450708.7:c.825-1_828delinsTACCTAGAGGTT
ENST00000478548.2:n.865-1_868delinsTACCTAGAGGTT
ENST00000671939.1:n.1102-1_1105delinsTACCTAGAGGTT
ENST00000671965.1:n.564_568delinsTACCTAGAGGTT
ENST00000672079.1:c.551-1_554delinsTACCTAGAGGTT
ENST00000672304.1:c.825-1_828delinsTACCTAGAGGTT
ENST00000312049.10:c.825-1_828delinsTACCTAGAGGTT
ENST00000315422.8:c.825-1_828delinsTACCTAGAGGTT
ENST00000337652.5:c.840-1_843delinsTACCTAGAGGTT
ENST00000377313.5:c.840-1_843delinsTACCTAGAGGTT
ENST00000377316.6:c.825-1_828delinsTACCTAGAGGTT
ENST00000377321.5:c.720-1_723delinsTACCTAGAGGTT
ENST00000377326.7:c.825-1_828delinsTACCTAGAGGTT
ENST00000394374.6:c.840-1_843delinsTACCTAGAGGTT
ENST00000394376.5:c.840-1_843delinsTACCTAGAGGTT
ENST00000440873.5:c.825-1_828delinsTACCTAGAGGTT
ENST00000450708.5:c.825-1_828delinsTACCTAGAGGTT
NM_000244.3:c.840-1_843delinsTACCTAGAGGTT , LRG_509t1:c.840-1_843delinsTACCTAGAGGTT
NM_130799.2:c.825-1_828delinsTACCTAGAGGTT , LRG_509t2:c.825-1_828delinsTACCTAGAGGTT
NM_130800.2:c.840-1_843delinsTACCTAGAGGTT
NM_130801.2:c.840-1_843delinsTACCTAGAGGTT
NM_130802.2:c.840-1_843delinsTACCTAGAGGTT
NM_130803.2:c.840-1_843delinsTACCTAGAGGTT
NM_130804.2:c.840-1_843delinsTACCTAGAGGTT
XM_005274001.3:c.825-1_828delinsTACCTAGAGGTT
XM_011545040.1:c.825-1_828delinsTACCTAGAGGTT
XM_011545041.1:c.825-1_828delinsTACCTAGAGGTT
XM_011545042.1:c.825-1_828delinsTACCTAGAGGTT
XM_005274001.4:c.825-1_828delinsTACCTAGAGGTT
XM_011545041.2:c.825-1_828delinsTACCTAGAGGTT
XM_011545042.3:c.825-1_828delinsTACCTAGAGGTT
XM_017017765.1:c.840-1_843delinsTACCTAGAGGTT
XM_017017766.1:c.840-1_843delinsTACCTAGAGGTT
XM_017017767.2:c.840-1_843delinsTACCTAGAGGTT
XM_017017768.1:c.840-1_843delinsTACCTAGAGGTT
XM_017017769.1:c.825-1_828delinsTACCTAGAGGTT
XM_017017770.2:c.825-1_828delinsTACCTAGAGGTT
NM_001370251.1:c.825-1_828delinsTACCTAGAGGTT
NM_001370259.2:c.825-1_828delinsTACCTAGAGGTT
NM_001370260.1:c.825-1_828delinsTACCTAGAGGTT
NM_001370261.1:c.825-1_828delinsTACCTAGAGGTT
NM_001370262.1:c.720-1_723delinsTACCTAGAGGTT
NM_001370263.1:c.720-1_723delinsTACCTAGAGGTT
NM_000244.4:c.840-1_843delinsTACCTAGAGGTT
NM_001370251.2:c.825-1_828delinsTACCTAGAGGTT
NM_001370260.2:c.825-1_828delinsTACCTAGAGGTT
NM_001370261.2:c.825-1_828delinsTACCTAGAGGTT
NM_001370262.2:c.720-1_723delinsTACCTAGAGGTT
NM_001370263.2:c.720-1_723delinsTACCTAGAGGTT
NM_130799.3:c.825-1_828delinsTACCTAGAGGTT
NM_130800.3:c.840-1_843delinsTACCTAGAGGTT
NM_130801.3:c.840-1_843delinsTACCTAGAGGTT
NM_130802.3:c.840-1_843delinsTACCTAGAGGTT
NM_130803.3:c.840-1_843delinsTACCTAGAGGTT
NM_130804.3:c.840-1_843delinsTACCTAGAGGTT