Canonical Allele Identifier: CA2629527970

Gene: MPI

Linked Data

• gnomAD v4: 15-74890803-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890804_74890805del , CM000677.2:g.74890804_74890805del	GRCh38
NC_000015.9:g.75183145_75183146del , CM000677.1:g.75183145_75183146del	GRCh37
NC_000015.8:g.72970198_72970199del	NCBI36
NG_008921.1:g.5736_5737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.144+150_144+151del MANE Select	ENSP00000318318.6:n.144+150_144+151del
ENST00000323744.10:c.144+150_144+151del	ENSP00000318192.6:n.144+150_144+151del
ENST00000352410.8:c.144+150_144+151del	ENSP00000318318.6:n.144+150_144+151del
ENST00000535694.5:c.-6-575_-6-574del	ENSP00000440447.1:n.-6-575_-6-574del
ENST00000561470.5:c.*40+150_*40+151del	ENSP00000454267.1:n.*40+150_*40+151del
ENST00000562606.5:c.84+150_84+151del	ENSP00000457020.1:n.84+150_84+151del
ENST00000562800.5:c.144+150_144+151del	ENSP00000457619.1:n.144+150_144+151del
ENST00000563422.5:c.144+150_144+151del	ENSP00000457885.1:n.144+150_144+151del
ENST00000563786.5:c.84+150_84+151del	ENSP00000455241.1:n.84+150_84+151del
ENST00000564003.5:c.-6-575_-6-574del	ENSP00000454312.1:n.-6-575_-6-574del
ENST00000564633.5:c.84+150_84+151del	ENSP00000455383.1:n.84+150_84+151del
ENST00000565576.5:c.144+150_144+151del	ENSP00000454619.1:n.144+150_144+151del
ENST00000566377.5:c.144+150_144+151del	ENSP00000455405.1:n.144+150_144+151del
ENST00000567116.5:n.175+150_175+151del
ENST00000567132.5:c.144+150_144+151del	ENSP00000455972.1:n.144+150_144+151del
ENST00000567177.1:c.105+150_105+151del	ENSP00000457013.1:n.105+150_105+151del
ENST00000567570.5:c.84+150_84+151del	ENSP00000455477.1:n.84+150_84+151del
ENST00000568303.1:n.411_412del
ENST00000568828.5:c.144+150_144+151del	ENSP00000455065.1:n.144+150_144+151del
ENST00000568840.1:n.253+150_253+151del
ENST00000568907.5:c.144+150_144+151del	ENSP00000457494.1:n.144+150_144+151del
ENST00000569233.5:c.144+150_144+151del	ENSP00000454622.1:n.144+150_144+151del
ENST00000569931.5:c.84+150_84+151del	ENSP00000455161.1:n.84+150_84+151del
NM_001289155.1:c.144+150_144+151del	NP_001276084.1:n.144+150_144+151del
NM_001289156.1:c.-6-575_-6-574del	NP_001276085.1:n.-6-575_-6-574del
NM_001289157.1:c.144+150_144+151del	NP_001276086.1:n.144+150_144+151del
NM_002435.2:c.144+150_144+151del	NP_002426.1:n.144+150_144+151del
XM_011521592.1:c.132+150_132+151del	XP_011519894.1:n.132+150_132+151del
XM_011521593.1:c.84+150_84+151del	XP_011519895.1:n.84+150_84+151del
NM_001330372.1:c.84+150_84+151del	NP_001317301.1:n.84+150_84+151del
XM_017022208.1:c.84+150_84+151del	XP_016877697.1:n.84+150_84+151del
XM_017022209.2:c.-6-575_-6-574del	XP_016877698.1:n.-6-575_-6-574del
NM_002435.3:c.144+150_144+151del MANE Select	NP_002426.1:n.144+150_144+151del
NM_001289155.2:c.144+150_144+151del	NP_001276084.1:n.144+150_144+151del
NM_001289156.2:c.-6-575_-6-574del	NP_001276085.1:n.-6-575_-6-574del
NM_001289157.2:c.144+150_144+151del	NP_001276086.1:n.144+150_144+151del
NM_001330372.2:c.84+150_84+151del	NP_001317301.1:n.84+150_84+151del