Canonical Allele Identifier: CA2629527106

Gene: MPI

Linked Data

• gnomAD v4: 15-74890305-TCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890307_74890309del , CM000677.2:g.74890307_74890309del	GRCh38
NC_000015.9:g.75182648_75182650del , CM000677.1:g.75182648_75182650del	GRCh37
NC_000015.8:g.72969701_72969703del	NCBI36
NG_008921.1:g.5239_5241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.16+218_17-218del MANE Select	ENSP00000318318.6:n.16+218_17-218del
ENST00000323744.10:c.16+218_17-218del	ENSP00000318192.6:n.16+218_17-218del
ENST00000352410.8:c.16+218_17-218del	ENSP00000318318.6:n.16+218_17-218del
ENST00000535694.5:c.-7+218_-7+220del	ENSP00000440447.1:n.-7+218_-7+220del
ENST00000561470.5:c.128+106_128+108del	ENSP00000454267.1:n.128+106_128+108del
ENST00000562606.5:c.-19+218_-19+220del	ENSP00000457020.1:n.-19+218_-19+220del
ENST00000562800.5:c.16+218_17-218del	ENSP00000457619.1:n.16+218_17-218del
ENST00000563422.5:c.16+218_17-218del	ENSP00000457885.1:n.16+218_17-218del
ENST00000563786.5:c.-133-131_-133-129del	ENSP00000455241.1:n.-133-131_-133-129del
ENST00000564003.5:c.-7+218_-7+220del	ENSP00000454312.1:n.-7+218_-7+220del
ENST00000564633.5:c.-16+218_-16+220del	ENSP00000455383.1:n.-16+218_-16+220del
ENST00000565576.5:c.16+218_17-218del	ENSP00000454619.1:n.16+218_17-218del
ENST00000566377.5:c.16+218_17-218del	ENSP00000455405.1:n.16+218_17-218del
ENST00000567116.5:n.47+218_48-218del
ENST00000567132.5:c.16+218_17-218del	ENSP00000455972.1:n.16+218_17-218del
ENST00000567570.5:c.-264_-262del	ENSP00000455477.1:n.-264_-262del
ENST00000568303.1:n.45-131_45-129del
ENST00000568828.5:c.16+218_17-218del	ENSP00000455065.1:n.16+218_17-218del
ENST00000568840.1:n.125+106_125+108del
ENST00000568907.5:c.16+218_17-218del	ENSP00000457494.1:n.16+218_17-218del
ENST00000569233.5:c.16+218_17-218del	ENSP00000454622.1:n.16+218_17-218del
ENST00000569931.5:c.-19+218_-19+220del	ENSP00000455161.1:n.-19+218_-19+220del
NM_001289155.1:c.16+218_17-218del	NP_001276084.1:n.16+218_17-218del
NM_001289156.1:c.-7+218_-7+220del	NP_001276085.1:n.-7+218_-7+220del
NM_001289157.1:c.16+218_17-218del	NP_001276086.1:n.16+218_17-218del
NM_002435.2:c.16+218_17-218del	NP_002426.1:n.16+218_17-218del
XM_011521592.1:c.4+106_4+108del	XP_011519894.1:n.4+106_4+108del
XM_011521593.1:c.-133-131_-133-129del	XP_011519895.1:n.-133-131_-133-129del
NM_001330372.1:c.-133-131_-133-129del	NP_001317301.1:n.-133-131_-133-129del
XM_017022208.1:c.-133-131_-133-129del	XP_016877697.1:n.-133-131_-133-129del
XM_017022209.2:c.-7+218_-7+220del	XP_016877698.1:n.-7+218_-7+220del
NM_002435.3:c.16+218_17-218del MANE Select	NP_002426.1:n.16+218_17-218del
NM_001289155.2:c.16+218_17-218del	NP_001276084.1:n.16+218_17-218del
NM_001289156.2:c.-7+218_-7+220del	NP_001276085.1:n.-7+218_-7+220del
NM_001289157.2:c.16+218_17-218del	NP_001276086.1:n.16+218_17-218del
NM_001330372.2:c.-133-131_-133-129del	NP_001317301.1:n.-133-131_-133-129del