Canonical Allele Identifier: CA7662417

Gene: MPI

Linked Data

• dbSNP Id: rs781601811
• ExAC: 15:75184973 ATCC / A
• gnomAD v4: 15-74892632-ATCC-A
• MyVariant Identifiers: chr15:g.75184974_75184976del (hg19) ; chr15:g.74892633_74892635del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74892638_74892640del , CM000677.2:g.74892638_74892640del	GRCh38
NC_000015.9:g.75184979_75184981del , CM000677.1:g.75184979_75184981del	GRCh37
NC_000015.8:g.72972032_72972034del	NCBI36
NG_008921.1:g.7570_7572del

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.346-23_346-21del MANE Select	ENSP00000318318.6:n.346-23_346-21del
ENST00000323744.10:c.346-23_346-21del	ENSP00000318192.6:n.346-23_346-21del
ENST00000352410.8:c.346-23_346-21del	ENSP00000318318.6:n.346-23_346-21del
ENST00000535694.5:c.196-23_196-21del	ENSP00000440447.1:n.196-23_196-21del
ENST00000561470.5:c.*242-23_*242-21del	ENSP00000454267.1:n.*242-23_*242-21del
ENST00000562606.5:c.286-23_286-21del	ENSP00000457020.1:n.286-23_286-21del
ENST00000562800.5:c.255+1149_255+1151del	ENSP00000457619.1:n.255+1149_255+1151del
ENST00000563422.5:c.346-23_346-21del	ENSP00000457885.1:n.346-23_346-21del
ENST00000563786.5:c.286-23_286-21del	ENSP00000455241.1:n.286-23_286-21del
ENST00000564003.5:c.196-23_196-21del	ENSP00000454312.1:n.196-23_196-21del
ENST00000564633.5:c.286-23_286-21del	ENSP00000455383.1:n.286-23_286-21del
ENST00000565576.5:c.346-23_346-21del	ENSP00000454619.1:n.346-23_346-21del
ENST00000566377.5:c.346-23_346-21del	ENSP00000455405.1:n.346-23_346-21del
ENST00000567116.5:n.377-23_377-21del
ENST00000567132.5:c.331-50_331-48del	ENSP00000455972.1:n.331-50_331-48del
ENST00000567177.1:c.307-23_307-21del	ENSP00000457013.1:n.307-23_307-21del
ENST00000567570.5:c.286-23_286-21del	ENSP00000455477.1:n.286-23_286-21del
ENST00000568828.5:c.310-23_310-21del	ENSP00000455065.1:n.310-23_310-21del
ENST00000568840.1:n.455-23_455-21del
ENST00000568907.5:c.256-23_256-21del	ENSP00000457494.1:n.256-23_256-21del
ENST00000569233.5:c.403-23_403-21del	ENSP00000454622.1:n.403-23_403-21del
ENST00000569931.5:c.286-23_286-21del	ENSP00000455161.1:n.286-23_286-21del
NM_001289155.1:c.346-23_346-21del	NP_001276084.1:n.346-23_346-21del
NM_001289156.1:c.196-23_196-21del	NP_001276085.1:n.196-23_196-21del
NM_001289157.1:c.346-23_346-21del	NP_001276086.1:n.346-23_346-21del
NM_002435.2:c.346-23_346-21del	NP_002426.1:n.346-23_346-21del
XM_011521592.1:c.334-23_334-21del	XP_011519894.1:n.334-23_334-21del
XM_011521593.1:c.286-23_286-21del	XP_011519895.1:n.286-23_286-21del
NM_001330372.1:c.286-23_286-21del	NP_001317301.1:n.286-23_286-21del
XM_017022208.1:c.286-23_286-21del	XP_016877697.1:n.286-23_286-21del
XM_017022209.2:c.196-23_196-21del	XP_016877698.1:n.196-23_196-21del
NM_002435.3:c.346-23_346-21del MANE Select	NP_002426.1:n.346-23_346-21del
NM_001289155.2:c.346-23_346-21del	NP_001276084.1:n.346-23_346-21del
NM_001289156.2:c.196-23_196-21del	NP_001276085.1:n.196-23_196-21del
NM_001289157.2:c.346-23_346-21del	NP_001276086.1:n.346-23_346-21del
NM_001330372.2:c.286-23_286-21del	NP_001317301.1:n.286-23_286-21del