Canonical Allele Identifier: CA11529665
Gene: MOBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39471787C>T , CM000665.2:g.39471787C>T GRCh38
NC_000003.11:g.39513278C>T , CM000665.1:g.39513278C>T GRCh37
NC_000003.10:g.39488282C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682069.1:c.-5+4047C>T ENSP00000506926.1:n.-5+4047C>T
ENST00000684792.1:c.-89+4047C>T MANE Select ENSP00000508923.1:n.-89+4047C>T
ENST00000311042.10:c.-89+4047C>T ENSP00000312293.6:n.-89+4047C>T
ENST00000383754.7:c.-89+4047C>T ENSP00000373261.3:n.-89+4047C>T
ENST00000415443.5:c.-71+4047C>T ENSP00000388148.1:n.-71+4047C>T
ENST00000420739.5:c.-89+4047C>T ENSP00000400491.1:n.-89+4047C>T
ENST00000428261.5:c.-155+4047C>T ENSP00000401312.1:n.-155+4047C>T
ENST00000436143.6:c.-323+4047C>T ENSP00000409071.2:n.-323+4047C>T
ENST00000441980.6:c.-71+4047C>T ENSP00000388827.2:n.-71+4047C>T
ENST00000447324.5:c.-5+4047C>T ENSP00000409730.1:n.-5+4047C>T
ENST00000451925.5:c.-89+4047C>T ENSP00000410720.1:n.-89+4047C>T
ENST00000452959.6:c.-89+4047C>T ENSP00000405549.1:n.-89+4047C>T
NM_001278322.1:c.-89+4047C>T NP_001265251.1:n.-89+4047C>T
NM_182935.3:c.-89+4047C>T NP_891980.1:n.-89+4047C>T
NR_003090.2:n.168+4047C>T
NR_103504.1:n.168+4047C>T
NR_103505.1:n.168+4047C>T
NR_103506.1:n.168+4047C>T
NM_001278322.2:c.-89+4047C>T NP_001265251.1:n.-89+4047C>T
NM_001278323.2:c.-5+4047C>T NP_001265252.1:n.-5+4047C>T
NM_182935.4:c.-89+4047C>T NP_891980.1:n.-89+4047C>T
NR_003090.3:n.61+4047C>T
NR_103504.2:n.61+4047C>T
NR_103505.2:n.61+4047C>T
NR_103506.2:n.61+4047C>T
NM_001393704.1:c.-89+4047C>T MANE Select NP_001380633.1:n.-89+4047C>T
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