Canonical Allele Identifier: CA2804770406

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890340_74890350del , CM000677.2:g.74890340_74890350del	GRCh38
NC_000015.9:g.75182681_75182691del , CM000677.1:g.75182681_75182691del	GRCh37
NC_000015.8:g.72969734_72969744del	NCBI36
NG_008921.1:g.5272_5282del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.17-187_17-177del MANE Select	ENSP00000318318.6:n.17-187_17-177del
ENST00000323744.10:c.17-187_17-177del	ENSP00000318192.6:n.17-187_17-177del
ENST00000352410.8:c.17-187_17-177del	ENSP00000318318.6:n.17-187_17-177del
ENST00000535694.5:c.-7+251_-7+261del	ENSP00000440447.1:n.-7+251_-7+261del
ENST00000561470.5:c.128+139_128+149del	ENSP00000454267.1:n.128+139_128+149del
ENST00000562606.5:c.-18-213_-18-203del	ENSP00000457020.1:n.-18-213_-18-203del
ENST00000562800.5:c.17-187_17-177del	ENSP00000457619.1:n.17-187_17-177del
ENST00000563422.5:c.17-187_17-177del	ENSP00000457885.1:n.17-187_17-177del
ENST00000563786.5:c.-133-98_-133-88del	ENSP00000455241.1:n.-133-98_-133-88del
ENST00000564003.5:c.-7+251_-7+261del	ENSP00000454312.1:n.-7+251_-7+261del
ENST00000564633.5:c.-15-216_-15-206del	ENSP00000455383.1:n.-15-216_-15-206del
ENST00000565576.5:c.17-187_17-177del	ENSP00000454619.1:n.17-187_17-177del
ENST00000566377.5:c.17-187_17-177del	ENSP00000455405.1:n.17-187_17-177del
ENST00000567116.5:n.48-187_48-177del
ENST00000567132.5:c.17-187_17-177del	ENSP00000455972.1:n.17-187_17-177del
ENST00000567570.5:c.-231_-221del	ENSP00000455477.1:n.-231_-221del
ENST00000568303.1:n.45-98_45-88del
ENST00000568828.5:c.17-187_17-177del	ENSP00000455065.1:n.17-187_17-177del
ENST00000568840.1:n.125+139_125+149del
ENST00000568907.5:c.17-187_17-177del	ENSP00000457494.1:n.17-187_17-177del
ENST00000569233.5:c.17-187_17-177del	ENSP00000454622.1:n.17-187_17-177del
ENST00000569931.5:c.-18-213_-18-203del	ENSP00000455161.1:n.-18-213_-18-203del
NM_001289155.1:c.17-187_17-177del	NP_001276084.1:n.17-187_17-177del
NM_001289156.1:c.-7+251_-7+261del	NP_001276085.1:n.-7+251_-7+261del
NM_001289157.1:c.17-187_17-177del	NP_001276086.1:n.17-187_17-177del
NM_002435.2:c.17-187_17-177del	NP_002426.1:n.17-187_17-177del
XM_011521592.1:c.4+139_4+149del	XP_011519894.1:n.4+139_4+149del
XM_011521593.1:c.-133-98_-133-88del	XP_011519895.1:n.-133-98_-133-88del
NM_001330372.1:c.-133-98_-133-88del	NP_001317301.1:n.-133-98_-133-88del
XM_017022208.1:c.-133-98_-133-88del	XP_016877697.1:n.-133-98_-133-88del
XM_017022209.2:c.-7+251_-7+261del	XP_016877698.1:n.-7+251_-7+261del
NM_002435.3:c.17-187_17-177del MANE Select	NP_002426.1:n.17-187_17-177del
NM_001289155.2:c.17-187_17-177del	NP_001276084.1:n.17-187_17-177del
NM_001289156.2:c.-7+251_-7+261del	NP_001276085.1:n.-7+251_-7+261del
NM_001289157.2:c.17-187_17-177del	NP_001276086.1:n.17-187_17-177del
NM_001330372.2:c.-133-98_-133-88del	NP_001317301.1:n.-133-98_-133-88del