Canonical Allele Identifier: CA2187894538

Gene: MPI

Linked Data

• dbSNP Id: rs2064706731

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890420_74890429del , CM000677.2:g.74890420_74890429del	GRCh38
NC_000015.9:g.75182761_75182770del , CM000677.1:g.75182761_75182770del	GRCh37
NC_000015.8:g.72969814_72969823del	NCBI36
NG_008921.1:g.5352_5361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.17-107_17-98del MANE Select	ENSP00000318318.6:n.17-107_17-98del
ENST00000323744.10:c.17-107_17-98del	ENSP00000318192.6:n.17-107_17-98del
ENST00000352410.8:c.17-107_17-98del	ENSP00000318318.6:n.17-107_17-98del
ENST00000535694.5:c.-7+331_-7+340del	ENSP00000440447.1:n.-7+331_-7+340del
ENST00000561470.5:c.129-107_129-98del	ENSP00000454267.1:n.129-107_129-98del
ENST00000562606.5:c.-18-133_-18-124del	ENSP00000457020.1:n.-18-133_-18-124del
ENST00000562800.5:c.17-107_17-98del	ENSP00000457619.1:n.17-107_17-98del
ENST00000563422.5:c.17-107_17-98del	ENSP00000457885.1:n.17-107_17-98del
ENST00000563786.5:c.-133-18_-133-9del	ENSP00000455241.1:n.-133-18_-133-9del
ENST00000564003.5:c.-7+331_-7+340del	ENSP00000454312.1:n.-7+331_-7+340del
ENST00000564633.5:c.-15-136_-15-127del	ENSP00000455383.1:n.-15-136_-15-127del
ENST00000565576.5:c.17-107_17-98del	ENSP00000454619.1:n.17-107_17-98del
ENST00000566377.5:c.17-107_17-98del	ENSP00000455405.1:n.17-107_17-98del
ENST00000567116.5:n.48-107_48-98del
ENST00000567132.5:c.17-107_17-98del	ENSP00000455972.1:n.17-107_17-98del
ENST00000567570.5:c.-151_-142del	ENSP00000455477.1:n.-151_-142del
ENST00000568303.1:n.45-18_45-9del
ENST00000568828.5:c.17-107_17-98del	ENSP00000455065.1:n.17-107_17-98del
ENST00000568840.1:n.126-107_126-98del
ENST00000568907.5:c.17-107_17-98del	ENSP00000457494.1:n.17-107_17-98del
ENST00000569233.5:c.17-107_17-98del	ENSP00000454622.1:n.17-107_17-98del
ENST00000569931.5:c.-18-133_-18-124del	ENSP00000455161.1:n.-18-133_-18-124del
NM_001289155.1:c.17-107_17-98del	NP_001276084.1:n.17-107_17-98del
NM_001289156.1:c.-7+331_-7+340del	NP_001276085.1:n.-7+331_-7+340del
NM_001289157.1:c.17-107_17-98del	NP_001276086.1:n.17-107_17-98del
NM_002435.2:c.17-107_17-98del	NP_002426.1:n.17-107_17-98del
XM_011521592.1:c.5-107_5-98del	XP_011519894.1:n.5-107_5-98del
XM_011521593.1:c.-133-18_-133-9del	XP_011519895.1:n.-133-18_-133-9del
NM_001330372.1:c.-133-18_-133-9del	NP_001317301.1:n.-133-18_-133-9del
XM_017022208.1:c.-133-18_-133-9del	XP_016877697.1:n.-133-18_-133-9del
XM_017022209.2:c.-7+331_-7+340del	XP_016877698.1:n.-7+331_-7+340del
NM_002435.3:c.17-107_17-98del MANE Select	NP_002426.1:n.17-107_17-98del
NM_001289155.2:c.17-107_17-98del	NP_001276084.1:n.17-107_17-98del
NM_001289156.2:c.-7+331_-7+340del	NP_001276085.1:n.-7+331_-7+340del
NM_001289157.2:c.17-107_17-98del	NP_001276086.1:n.17-107_17-98del
NM_001330372.2:c.-133-18_-133-9del	NP_001317301.1:n.-133-18_-133-9del