Canonical Allele Identifier: CA916083244

Gene: MEN1

Linked Data

• ClinVar Variation Id: 844638
• ClinVar RCV Id: RCV001047541
• dbSNP Id: rs1941598294

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64805008_64805109del , CM000673.2:g.64805008_64805109del	GRCh38
NC_000011.9:g.64572480_64572581del , CM000673.1:g.64572480_64572581del	GRCh37
NC_000011.8:g.64329056_64329157del	NCBI36
NG_033040.1:g.3135_3236del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377313.7:c.1292_1365+28del
ENST00000394374.8:c.*585_*658+28del
ENST00000394376.7:c.1277_1350+28del
ENST00000413626.2:c.1277_1350+28del
ENST00000424912.2:c.1277_1350+28del
ENST00000429702.6:c.1277_1350+28del
ENST00000672079.2:c.*373_*446+28del
ENST00000710881.1:c.1292_1365+28del
ENST00000394374.7:c.1024_1097+28del
ENST00000394376.6:c.628_701+28del
ENST00000478548.3:n.1770_1843+28del
ENST00000671939.2:n.1239_1312+28del
ENST00000671965.2:n.1659_1732+28del
ENST00000312049.11:c.1277_1350+28del
ENST00000315422.9:c.1277_1350+28del
ENST00000377313.6:c.1292_1365+28del
ENST00000440873.6:c.1277_1350+28del
ENST00000450708.7:c.1277_1350+28del
ENST00000478548.2:n.1778_1851+28del
ENST00000671939.1:n.1554_1627+28del
ENST00000672079.1:c.1152_1225+28del
ENST00000672304.1:c.1403_1476+28del
ENST00000312049.10:c.1277_1350+28del
ENST00000315422.8:c.1277_1350+28del
ENST00000337652.5:c.1292_1365+28del
ENST00000377313.5:c.1292_1365+28del
ENST00000377316.6:c.1186-291_1186-190del	ENSP00000366533.1:n.1186-291_1186-190del
ENST00000377321.5:c.1172_1245+28del
ENST00000377326.7:c.1277_1350+28del
ENST00000394374.6:c.1292_1365+28del
ENST00000394376.5:c.1292_1365+28del
ENST00000478548.1:n.826_899+28del
XM_005274001.3:c.1277_1350+28del
XM_011545040.1:c.1403_1476+28del
XM_011545041.1:c.1403_1476+28del
XM_011545042.1:c.1403_1476+28del
XM_005274001.4:c.1277_1350+28del
XM_011545041.2:c.1403_1476+28del
XM_011545042.3:c.1403_1476+28del
XM_017017765.1:c.1418_1491+28del
XM_017017766.1:c.1418_1491+28del
XM_017017767.2:c.1418_1491+28del
XM_017017768.1:c.1418_1491+28del
XM_017017769.1:c.1277_1350+28del
XM_017017770.2:c.1277_1350+28del
NM_001370259.2:c.1277_1350+28del
NM_000244.4:c.1292_1365+28del
NM_001370251.2:c.1403_1476+28del
NM_001370260.2:c.1277_1350+28del
NM_001370261.2:c.1277_1350+28del
NM_001370262.2:c.1172_1245+28del
NM_001370263.2:c.1172_1245+28del
NM_130799.3:c.1277_1350+28del
NM_130800.3:c.1292_1365+28del
NM_130801.3:c.1292_1365+28del
NM_130802.3:c.1292_1365+28del
NM_130803.3:c.1292_1365+28del
NM_130804.3:c.1292_1365+28del