Canonical Allele Identifier: CA15229419

Gene: MOBP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39481512T>C , CM000665.2:g.39481512T>C	GRCh38
NC_000003.11:g.39523003T>C , CM000665.1:g.39523003T>C	GRCh37
NC_000003.10:g.39498007T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682069.1:c.-5+13772T>C	ENSP00000506926.1:n.-5+13772T>C
ENST00000684792.1:c.-5+1389T>C MANE Select	ENSP00000508923.1:n.-5+1389T>C
ENST00000311042.10:c.-5+1389T>C	ENSP00000312293.6:n.-5+1389T>C
ENST00000383754.7:c.-5+1389T>C	ENSP00000373261.3:n.-5+1389T>C
ENST00000415443.5:c.-71+13772T>C	ENSP00000388148.1:n.-71+13772T>C
ENST00000420739.5:c.-5+1389T>C	ENSP00000400491.1:n.-5+1389T>C
ENST00000428261.5:c.-71+1389T>C	ENSP00000401312.1:n.-71+1389T>C
ENST00000436143.6:c.-239+1389T>C	ENSP00000409071.2:n.-239+1389T>C
ENST00000441980.6:c.-71+13772T>C	ENSP00000388827.2:n.-71+13772T>C
ENST00000447324.5:c.-5+13772T>C	ENSP00000409730.1:n.-5+13772T>C
ENST00000451925.5:c.-5+1389T>C	ENSP00000410720.1:n.-5+1389T>C
ENST00000452959.6:c.-5+1389T>C	ENSP00000405549.1:n.-5+1389T>C
NM_001278322.1:c.-5+1389T>C	NP_001265251.1:n.-5+1389T>C
NM_182935.3:c.-5+1389T>C	NP_891980.1:n.-5+1389T>C
NR_003090.2:n.252+1389T>C
NR_103504.1:n.252+1389T>C
NR_103505.1:n.252+1389T>C
NR_103506.1:n.252+1389T>C
NM_001278322.2:c.-5+1389T>C	NP_001265251.1:n.-5+1389T>C
NM_001278323.2:c.-5+13772T>C	NP_001265252.1:n.-5+13772T>C
NM_182935.4:c.-5+1389T>C	NP_891980.1:n.-5+1389T>C
NR_003090.3:n.145+1389T>C
NR_103504.2:n.145+1389T>C
NR_103505.2:n.145+1389T>C
NR_103506.2:n.145+1389T>C
NM_001393704.1:c.-5+1389T>C MANE Select	NP_001380633.1:n.-5+1389T>C