Canonical Allele Identifier: CA1358992882

Gene: MOBP

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39512297C>G , CM000665.2:g.39512297C>G	GRCh38
NC_000003.11:g.39553788C>G , CM000665.1:g.39553788C>G	GRCh37
NC_000003.10:g.39528792C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311042.10:c.621-1086C>G	ENSP00000312293.6:n.621-1086C>G
ENST00000383754.7:c.207-1086C>G	ENSP00000373261.3:n.207-1086C>G
ENST00000415443.5:c.207-1086C>G	ENSP00000388148.1:n.207-1086C>G
ENST00000420739.5:c.*35-1086C>G	ENSP00000400491.1:n.*35-1086C>G
ENST00000424090.5:c.*35-1086C>G	ENSP00000389055.1:n.*35-1086C>G
ENST00000428261.5:c.207-1086C>G	ENSP00000401312.1:n.207-1086C>G
ENST00000442631.5:c.549-1086C>G	ENSP00000413771.1:n.549-1086C>G
ENST00000447324.5:c.207-1086C>G	ENSP00000409730.1:n.207-1086C>G
ENST00000452959.6:c.207-1086C>G	ENSP00000405549.1:n.207-1086C>G
ENST00000479860.1:n.62-1086C>G
NM_001278322.1:c.621-1086C>G	NP_001265251.1:n.621-1086C>G
NM_182935.3:c.207-1086C>G	NP_891980.1:n.207-1086C>G
NR_003090.2:n.463-1086C>G
NR_103504.1:n.805-1086C>G
NR_103505.1:n.843-1086C>G
NR_103506.1:n.253-1086C>G
NM_001278322.2:c.621-1086C>G	NP_001265251.1:n.621-1086C>G
NM_182935.4:c.207-1086C>G	NP_891980.1:n.207-1086C>G
NR_003090.3:n.356-1086C>G
NR_103504.2:n.698-1086C>G
NR_103505.2:n.736-1086C>G
NR_103506.2:n.146-1086C>G