Canonical Allele Identifier: CA2629527627

Gene: MPI

Linked Data

• ClinVar Variation Id: 3016439
• ClinVar RCV Id: RCV003876590
• gnomAD v4: 15-74890631-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890632del , CM000677.2:g.74890632del	GRCh38
NC_000015.9:g.75182973del , CM000677.1:g.75182973del	GRCh37
NC_000015.8:g.72970026del	NCBI36
NG_008921.1:g.5564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.122del MANE Select	ENSP00000318318.6:p.Ala41GlufsTer?
ENST00000323744.10:c.122del	ENSP00000318192.6:p.Ala41GlufsTer?
ENST00000352410.8:c.122del	ENSP00000318318.6:p.Ala41GlufsTer?
ENST00000535694.5:c.-7+543del	ENSP00000440447.1:n.-7+543del
ENST00000561470.5:c.*18del	ENSP00000454267.1:n.*18del
ENST00000562606.5:c.62del	ENSP00000457020.1:p.Ala21GlufsTer?
ENST00000562800.5:c.122del	ENSP00000457619.1:p.Ala41GlufsTer?
ENST00000563422.5:c.122del	ENSP00000457885.1:p.Ala41GlufsTer?
ENST00000563786.5:c.62del	ENSP00000455241.1:p.Ala21GlufsTer?
ENST00000564003.5:c.-7+543del	ENSP00000454312.1:n.-7+543del
ENST00000564633.5:c.62del	ENSP00000455383.1:p.Ala21GlufsTer?
ENST00000565576.5:c.122del	ENSP00000454619.1:p.Ala41GlufsTer?
ENST00000566377.5:c.122del	ENSP00000455405.1:p.Ala41GlufsTer?
ENST00000567116.5:n.153del
ENST00000567132.5:c.122del	ENSP00000455972.1:p.Ala41GlufsTer?
ENST00000567177.1:c.83del	ENSP00000457013.1:p.Ala28GlufsTer?
ENST00000567570.5:c.62del	ENSP00000455477.1:p.Ala21GlufsTer?
ENST00000568303.1:n.239del
ENST00000568828.5:c.122del	ENSP00000455065.1:p.Ala41GlufsTer19
ENST00000568840.1:n.231del
ENST00000568907.5:c.122del	ENSP00000457494.1:p.Ala41GlufsTer?
ENST00000569233.5:c.122del	ENSP00000454622.1:p.Ala41GlufsTer15
ENST00000569931.5:c.62del	ENSP00000455161.1:p.Ala21GlufsTer?
NM_001289155.1:c.122del	NP_001276084.1:p.Ala41GlufsTer?
NM_001289156.1:c.-7+543del	NP_001276085.1:n.-7+543del
NM_001289157.1:c.122del	NP_001276086.1:p.Ala41GlufsTer?
NM_002435.2:c.122del	NP_002426.1:p.Ala41GlufsTer?
XM_011521592.1:c.110del	XP_011519894.1:p.Ala37GlufsTer?
XM_011521593.1:c.62del	XP_011519895.1:p.Ala21GlufsTer?
NM_001330372.1:c.62del	NP_001317301.1:p.Ala21GlufsTer?
XM_017022208.1:c.62del	XP_016877697.1:p.Ala21GlufsTer?
XM_017022209.2:c.-7+543del	XP_016877698.1:n.-7+543del
NM_002435.3:c.122del MANE Select	NP_002426.1:p.Ala41GlufsTer?
NM_001289155.2:c.122del	NP_001276084.1:p.Ala41GlufsTer?
NM_001289156.2:c.-7+543del	NP_001276085.1:n.-7+543del
NM_001289157.2:c.122del	NP_001276086.1:p.Ala41GlufsTer?
NM_001330372.2:c.62del	NP_001317301.1:p.Ala21GlufsTer?