Canonical Allele Identifier: CA2187894966

Gene: MPI

Linked Data

• dbSNP Id: rs2064713807

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890722_74890723del , CM000677.2:g.74890722_74890723del	GRCh38
NC_000015.9:g.75183063_75183064del , CM000677.1:g.75183063_75183064del	GRCh37
NC_000015.8:g.72970116_72970117del	NCBI36
NG_008921.1:g.5654_5655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.144+68_144+69del MANE Select	ENSP00000318318.6:n.144+68_144+69del
ENST00000323744.10:c.144+68_144+69del	ENSP00000318192.6:n.144+68_144+69del
ENST00000352410.8:c.144+68_144+69del	ENSP00000318318.6:n.144+68_144+69del
ENST00000535694.5:c.-7+633_-7+634del	ENSP00000440447.1:n.-7+633_-7+634del
ENST00000561470.5:c.*40+68_*40+69del	ENSP00000454267.1:n.*40+68_*40+69del
ENST00000562606.5:c.84+68_84+69del	ENSP00000457020.1:n.84+68_84+69del
ENST00000562800.5:c.144+68_144+69del	ENSP00000457619.1:n.144+68_144+69del
ENST00000563422.5:c.144+68_144+69del	ENSP00000457885.1:n.144+68_144+69del
ENST00000563786.5:c.84+68_84+69del	ENSP00000455241.1:n.84+68_84+69del
ENST00000564003.5:c.-7+633_-7+634del	ENSP00000454312.1:n.-7+633_-7+634del
ENST00000564633.5:c.84+68_84+69del	ENSP00000455383.1:n.84+68_84+69del
ENST00000565576.5:c.144+68_144+69del	ENSP00000454619.1:n.144+68_144+69del
ENST00000566377.5:c.144+68_144+69del	ENSP00000455405.1:n.144+68_144+69del
ENST00000567116.5:n.175+68_175+69del
ENST00000567132.5:c.144+68_144+69del	ENSP00000455972.1:n.144+68_144+69del
ENST00000567177.1:c.105+68_105+69del	ENSP00000457013.1:n.105+68_105+69del
ENST00000567570.5:c.84+68_84+69del	ENSP00000455477.1:n.84+68_84+69del
ENST00000568303.1:n.329_330del
ENST00000568828.5:c.144+68_144+69del	ENSP00000455065.1:n.144+68_144+69del
ENST00000568840.1:n.253+68_253+69del
ENST00000568907.5:c.144+68_144+69del	ENSP00000457494.1:n.144+68_144+69del
ENST00000569233.5:c.144+68_144+69del	ENSP00000454622.1:n.144+68_144+69del
ENST00000569931.5:c.84+68_84+69del	ENSP00000455161.1:n.84+68_84+69del
NM_001289155.1:c.144+68_144+69del	NP_001276084.1:n.144+68_144+69del
NM_001289156.1:c.-7+633_-7+634del	NP_001276085.1:n.-7+633_-7+634del
NM_001289157.1:c.144+68_144+69del	NP_001276086.1:n.144+68_144+69del
NM_002435.2:c.144+68_144+69del	NP_002426.1:n.144+68_144+69del
XM_011521592.1:c.132+68_132+69del	XP_011519894.1:n.132+68_132+69del
XM_011521593.1:c.84+68_84+69del	XP_011519895.1:n.84+68_84+69del
NM_001330372.1:c.84+68_84+69del	NP_001317301.1:n.84+68_84+69del
XM_017022208.1:c.84+68_84+69del	XP_016877697.1:n.84+68_84+69del
XM_017022209.2:c.-7+633_-7+634del	XP_016877698.1:n.-7+633_-7+634del
NM_002435.3:c.144+68_144+69del MANE Select	NP_002426.1:n.144+68_144+69del
NM_001289155.2:c.144+68_144+69del	NP_001276084.1:n.144+68_144+69del
NM_001289156.2:c.-7+633_-7+634del	NP_001276085.1:n.-7+633_-7+634del
NM_001289157.2:c.144+68_144+69del	NP_001276086.1:n.144+68_144+69del
NM_001330372.2:c.84+68_84+69del	NP_001317301.1:n.84+68_84+69del