Canonical Allele Identifier: CA2739269590

Gene: MPI

Linked Data

• ClinVar Variation Id: 2854573
• ClinVar RCV Id: RCV003630948

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896993dup , CM000677.2:g.74896993dup	GRCh38
NC_000015.9:g.75189334dup , CM000677.1:g.75189334dup	GRCh37
NC_000015.8:g.72976387dup	NCBI36
NG_008921.1:g.11925dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.845-18dup MANE Select	ENSP00000318318.6:n.845-18dup
ENST00000323744.10:c.662-18dup	ENSP00000318192.6:n.662-18dup
ENST00000352410.8:c.845-18dup	ENSP00000318318.6:n.845-18dup
ENST00000535694.5:c.695-18dup	ENSP00000440447.1:n.695-18dup
ENST00000562800.5:c.256-546dup	ENSP00000457619.1:n.256-546dup
ENST00000563786.5:c.785-18dup	ENSP00000455241.1:n.785-18dup
ENST00000566377.5:c.845-519dup	ENSP00000455405.1:n.845-519dup
ENST00000566556.1:n.1560dup
ENST00000567177.1:c.623-519dup	ENSP00000457013.1:n.623-519dup
ENST00000569931.5:c.785-18dup	ENSP00000455161.1:n.785-18dup
NM_001289155.1:c.845-519dup	NP_001276084.1:n.845-519dup
NM_001289156.1:c.695-18dup	NP_001276085.1:n.695-18dup
NM_001289157.1:c.662-18dup	NP_001276086.1:n.662-18dup
NM_002435.2:c.845-18dup	NP_002426.1:n.845-18dup
XM_011521592.1:c.833-18dup	XP_011519894.1:n.833-18dup
XM_011521593.1:c.785-18dup	XP_011519895.1:n.785-18dup
NM_001330372.1:c.785-18dup	NP_001317301.1:n.785-18dup
XM_017022208.1:c.785-519dup	XP_016877697.1:n.785-519dup
XM_017022209.2:c.695-519dup	XP_016877698.1:n.695-519dup
NM_002435.3:c.845-18dup MANE Select	NP_002426.1:n.845-18dup
NM_001289155.2:c.845-519dup	NP_001276084.1:n.845-519dup
NM_001289156.2:c.695-18dup	NP_001276085.1:n.695-18dup
NM_001289157.2:c.662-18dup	NP_001276086.1:n.662-18dup
NM_001330372.2:c.785-18dup	NP_001317301.1:n.785-18dup