Canonical Allele Identifier: CA2629527625

Gene: MPI

Linked Data

• gnomAD v4: 15-74890631-G-GGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890631_74890632insGCC , CM000677.2:g.74890631_74890632insGCC	GRCh38
NC_000015.9:g.75182972_75182973insGCC , CM000677.1:g.75182972_75182973insGCC	GRCh37
NC_000015.8:g.72970025_72970026insGCC	NCBI36
NG_008921.1:g.5563_5564insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.121_122insGCC MANE Select	ENSP00000318318.6:p.Ala41delinsGlyPro
ENST00000323744.10:c.121_122insGCC	ENSP00000318192.6:p.Ala41delinsGlyPro
ENST00000352410.8:c.121_122insGCC	ENSP00000318318.6:p.Ala41delinsGlyPro
ENST00000535694.5:c.-7+542_-7+543insGCC	ENSP00000440447.1:n.-7+542_-7+543insGCC
ENST00000561470.5:c.*17_*18insGCC	ENSP00000454267.1:n.*17_*18insGCC
ENST00000562606.5:c.61_62insGCC	ENSP00000457020.1:p.Ala21delinsGlyPro
ENST00000562800.5:c.121_122insGCC	ENSP00000457619.1:p.Ala41delinsGlyPro
ENST00000563422.5:c.121_122insGCC	ENSP00000457885.1:p.Ala41delinsGlyPro
ENST00000563786.5:c.61_62insGCC	ENSP00000455241.1:p.Ala21delinsGlyPro
ENST00000564003.5:c.-7+542_-7+543insGCC	ENSP00000454312.1:n.-7+542_-7+543insGCC
ENST00000564633.5:c.61_62insGCC	ENSP00000455383.1:p.Ala21delinsGlyPro
ENST00000565576.5:c.121_122insGCC	ENSP00000454619.1:p.Ala41delinsGlyPro
ENST00000566377.5:c.121_122insGCC	ENSP00000455405.1:p.Ala41delinsGlyPro
ENST00000567116.5:n.152_153insGCC
ENST00000567132.5:c.121_122insGCC	ENSP00000455972.1:p.Ala41delinsGlyPro
ENST00000567177.1:c.82_83insGCC	ENSP00000457013.1:p.Ala28delinsGlyPro
ENST00000567570.5:c.61_62insGCC	ENSP00000455477.1:p.Ala21delinsGlyPro
ENST00000568303.1:n.238_239insGCC
ENST00000568828.5:c.121_122insGCC	ENSP00000455065.1:p.Ala41delinsGlyPro
ENST00000568840.1:n.230_231insGCC
ENST00000568907.5:c.121_122insGCC	ENSP00000457494.1:p.Ala41delinsGlyPro
ENST00000569233.5:c.121_122insGCC	ENSP00000454622.1:p.Ala41delinsGlyPro
ENST00000569931.5:c.61_62insGCC	ENSP00000455161.1:p.Ala21delinsGlyPro
NM_001289155.1:c.121_122insGCC	NP_001276084.1:p.Ala41delinsGlyPro
NM_001289156.1:c.-7+542_-7+543insGCC	NP_001276085.1:n.-7+542_-7+543insGCC
NM_001289157.1:c.121_122insGCC	NP_001276086.1:p.Ala41delinsGlyPro
NM_002435.2:c.121_122insGCC	NP_002426.1:p.Ala41delinsGlyPro
XM_011521592.1:c.109_110insGCC	XP_011519894.1:p.Ala37delinsGlyPro
XM_011521593.1:c.61_62insGCC	XP_011519895.1:p.Ala21delinsGlyPro
NM_001330372.1:c.61_62insGCC	NP_001317301.1:p.Ala21delinsGlyPro
XM_017022208.1:c.61_62insGCC	XP_016877697.1:p.Ala21delinsGlyPro
XM_017022209.2:c.-7+542_-7+543insGCC	XP_016877698.1:n.-7+542_-7+543insGCC
NM_002435.3:c.121_122insGCC MANE Select	NP_002426.1:p.Ala41delinsGlyPro
NM_001289155.2:c.121_122insGCC	NP_001276084.1:p.Ala41delinsGlyPro
NM_001289156.2:c.-7+542_-7+543insGCC	NP_001276085.1:n.-7+542_-7+543insGCC
NM_001289157.2:c.121_122insGCC	NP_001276086.1:p.Ala41delinsGlyPro
NM_001330372.2:c.61_62insGCC	NP_001317301.1:p.Ala21delinsGlyPro