Canonical Allele Identifier: CA2629529264

Gene: MPI

Linked Data

• gnomAD v4: 15-74892637-CCTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74892639_74892643del , CM000677.2:g.74892639_74892643del	GRCh38
NC_000015.9:g.75184980_75184984del , CM000677.1:g.75184980_75184984del	GRCh37
NC_000015.8:g.72972033_72972037del	NCBI36
NG_008921.1:g.7571_7575del

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.346-22_346-18del MANE Select	ENSP00000318318.6:n.346-22_346-18del
ENST00000323744.10:c.346-22_346-18del	ENSP00000318192.6:n.346-22_346-18del
ENST00000352410.8:c.346-22_346-18del	ENSP00000318318.6:n.346-22_346-18del
ENST00000535694.5:c.196-22_196-18del	ENSP00000440447.1:n.196-22_196-18del
ENST00000561470.5:c.*242-22_*242-18del	ENSP00000454267.1:n.*242-22_*242-18del
ENST00000562606.5:c.286-22_286-18del	ENSP00000457020.1:n.286-22_286-18del
ENST00000562800.5:c.255+1150_255+1154del	ENSP00000457619.1:n.255+1150_255+1154del
ENST00000563422.5:c.346-22_346-18del	ENSP00000457885.1:n.346-22_346-18del
ENST00000563786.5:c.286-22_286-18del	ENSP00000455241.1:n.286-22_286-18del
ENST00000564003.5:c.196-22_196-18del	ENSP00000454312.1:n.196-22_196-18del
ENST00000564633.5:c.286-22_286-18del	ENSP00000455383.1:n.286-22_286-18del
ENST00000565576.5:c.346-22_346-18del	ENSP00000454619.1:n.346-22_346-18del
ENST00000566377.5:c.346-22_346-18del	ENSP00000455405.1:n.346-22_346-18del
ENST00000567116.5:n.377-22_377-18del
ENST00000567132.5:c.331-49_331-45del	ENSP00000455972.1:n.331-49_331-45del
ENST00000567177.1:c.307-22_307-18del	ENSP00000457013.1:n.307-22_307-18del
ENST00000567570.5:c.286-22_286-18del	ENSP00000455477.1:n.286-22_286-18del
ENST00000568828.5:c.310-22_310-18del	ENSP00000455065.1:n.310-22_310-18del
ENST00000568840.1:n.455-22_455-18del
ENST00000568907.5:c.256-22_256-18del	ENSP00000457494.1:n.256-22_256-18del
ENST00000569233.5:c.403-22_403-18del	ENSP00000454622.1:n.403-22_403-18del
ENST00000569931.5:c.286-22_286-18del	ENSP00000455161.1:n.286-22_286-18del
NM_001289155.1:c.346-22_346-18del	NP_001276084.1:n.346-22_346-18del
NM_001289156.1:c.196-22_196-18del	NP_001276085.1:n.196-22_196-18del
NM_001289157.1:c.346-22_346-18del	NP_001276086.1:n.346-22_346-18del
NM_002435.2:c.346-22_346-18del	NP_002426.1:n.346-22_346-18del
XM_011521592.1:c.334-22_334-18del	XP_011519894.1:n.334-22_334-18del
XM_011521593.1:c.286-22_286-18del	XP_011519895.1:n.286-22_286-18del
NM_001330372.1:c.286-22_286-18del	NP_001317301.1:n.286-22_286-18del
XM_017022208.1:c.286-22_286-18del	XP_016877697.1:n.286-22_286-18del
XM_017022209.2:c.196-22_196-18del	XP_016877698.1:n.196-22_196-18del
NM_002435.3:c.346-22_346-18del MANE Select	NP_002426.1:n.346-22_346-18del
NM_001289155.2:c.346-22_346-18del	NP_001276084.1:n.346-22_346-18del
NM_001289156.2:c.196-22_196-18del	NP_001276085.1:n.196-22_196-18del
NM_001289157.2:c.346-22_346-18del	NP_001276086.1:n.346-22_346-18del
NM_001330372.2:c.286-22_286-18del	NP_001317301.1:n.286-22_286-18del