Canonical Allele Identifier: CA1978914256

Gene: MEN1

Linked Data

• dbSNP Id: rs1941412091

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64803515del , CM000673.2:g.64803515del	GRCh38
NC_000011.9:g.64570987del , CM000673.1:g.64570987del	GRCh37
NC_000011.8:g.64327563del	NCBI36
NG_008929.1:g.12780del , LRG_509:g.12780del
NG_033040.1:g.4727del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315422.9:c.*819del	ENSP00000323747.4:n.*819del
ENST00000377313.6:c.*819del	ENSP00000366530.1:n.*819del
ENST00000377316.6:c.*819del	ENSP00000366533.1:n.*819del
NM_000244.3:c.*819del , LRG_509t1:c.*819del	NP_000235.2:n.*819del
NM_130799.2:c.*819del , LRG_509t2:c.*819del	NP_570711.1:n.*819del
NM_130800.2:c.*819del	NP_570712.1:n.*819del
NM_130801.2:c.*819del	NP_570713.1:n.*819del
NM_130802.2:c.*819del	NP_570714.1:n.*819del
NM_130803.2:c.*819del	NP_570715.1:n.*819del
NM_130804.2:c.*819del	NP_570716.1:n.*819del
XM_005274001.3:c.*819del	XP_005274058.1:n.*819del
NM_001370251.1:c.*819del	NP_001357180.1:n.*819del
NM_001370260.1:c.*819del	NP_001357189.1:n.*819del
NM_001370261.1:c.*819del	NP_001357190.1:n.*819del
NM_001370262.1:c.*819del	NP_001357191.1:n.*819del
NM_001370263.1:c.*819del	NP_001357192.1:n.*819del