Canonical Allele Identifier: CA619413160

Gene: MPI

Linked Data

• ClinVar Variation Id: 1990742
• ClinVar RCV Id: RCV002805808
• dbSNP Id: rs1268293635
• gnomAD v2: 15-75188661-AAGG-A
• gnomAD v4: 15-74896320-AAGG-A
• MyVariant Identifiers: chr15:g.75188662_75188664del (hg19) ; chr15:g.74896321_74896323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896324_74896326del , CM000677.2:g.74896324_74896326del	GRCh38
NC_000015.9:g.75188665_75188667del , CM000677.1:g.75188665_75188667del	GRCh37
NC_000015.8:g.72975718_72975720del	NCBI36
NG_008921.1:g.11256_11258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.843_844+1del
ENST00000323744.10:c.660_661+1del
ENST00000352410.8:c.843_844+1del
ENST00000535694.5:c.693_694+1del
ENST00000562606.5:c.783_785del	ENSP00000457020.1:p.Gly262del
ENST00000562800.5:c.256-1215_256-1213del	ENSP00000457619.1:n.256-1215_256-1213del
ENST00000563422.5:c.843_845del	ENSP00000457885.1:p.Gly282del
ENST00000563786.5:c.783_784+1del
ENST00000564003.5:c.510_512del	ENSP00000454312.1:p.Gly171del
ENST00000566377.5:c.843_844+1del
ENST00000566556.1:n.891_893del
ENST00000567177.1:c.621_622+1del
ENST00000569931.5:c.783_784+1del
NM_001289155.1:c.843_844+1del
NM_001289156.1:c.693_694+1del
NM_001289157.1:c.660_661+1del
NM_002435.2:c.843_844+1del
XM_011521592.1:c.831_832+1del
XM_011521593.1:c.783_784+1del
NM_001330372.1:c.783_784+1del
XM_017022208.1:c.783_784+1del
XM_017022209.2:c.693_694+1del
NM_002435.3:c.843_844+1del
NM_001289155.2:c.843_844+1del
NM_001289156.2:c.693_694+1del
NM_001289157.2:c.660_661+1del
NM_001330372.2:c.783_784+1del