Canonical Allele Identifier: CA272821576

Gene: MPI

Linked Data

• dbSNP Id: rs35459900
• gnomAD v2: 15-75182727-A-AG
• gnomAD v3: 15-74890386-A-AG
• gnomAD v4: 15-74890386-A-AG
• MyVariant Identifiers: chr15:g.75182727_75182728insG (hg19) ; chr15:g.74890386_74890387insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890392dup , CM000677.2:g.74890392dup	GRCh38
NC_000015.9:g.75182733dup , CM000677.1:g.75182733dup	GRCh37
NC_000015.8:g.72969786dup	NCBI36
NG_008921.1:g.5324dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.17-135dup MANE Select	ENSP00000318318.6:n.17-135dup
ENST00000323744.10:c.17-135dup	ENSP00000318192.6:n.17-135dup
ENST00000352410.8:c.17-135dup	ENSP00000318318.6:n.17-135dup
ENST00000535694.5:c.-7+303dup	ENSP00000440447.1:n.-7+303dup
ENST00000561470.5:c.129-135dup	ENSP00000454267.1:n.129-135dup
ENST00000562606.5:c.-18-161dup	ENSP00000457020.1:n.-18-161dup
ENST00000562800.5:c.17-135dup	ENSP00000457619.1:n.17-135dup
ENST00000563422.5:c.17-135dup	ENSP00000457885.1:n.17-135dup
ENST00000563786.5:c.-133-46dup	ENSP00000455241.1:n.-133-46dup
ENST00000564003.5:c.-7+303dup	ENSP00000454312.1:n.-7+303dup
ENST00000564633.5:c.-15-164dup	ENSP00000455383.1:n.-15-164dup
ENST00000565576.5:c.17-135dup	ENSP00000454619.1:n.17-135dup
ENST00000566377.5:c.17-135dup	ENSP00000455405.1:n.17-135dup
ENST00000567116.5:n.48-135dup
ENST00000567132.5:c.17-135dup	ENSP00000455972.1:n.17-135dup
ENST00000567570.5:c.-179dup	ENSP00000455477.1:n.-179dup
ENST00000568303.1:n.45-46dup
ENST00000568828.5:c.17-135dup	ENSP00000455065.1:n.17-135dup
ENST00000568840.1:n.126-135dup
ENST00000568907.5:c.17-135dup	ENSP00000457494.1:n.17-135dup
ENST00000569233.5:c.17-135dup	ENSP00000454622.1:n.17-135dup
ENST00000569931.5:c.-18-161dup	ENSP00000455161.1:n.-18-161dup
NM_001289155.1:c.17-135dup	NP_001276084.1:n.17-135dup
NM_001289156.1:c.-7+303dup	NP_001276085.1:n.-7+303dup
NM_001289157.1:c.17-135dup	NP_001276086.1:n.17-135dup
NM_002435.2:c.17-135dup	NP_002426.1:n.17-135dup
XM_011521592.1:c.5-135dup	XP_011519894.1:n.5-135dup
XM_011521593.1:c.-133-46dup	XP_011519895.1:n.-133-46dup
NM_001330372.1:c.-133-46dup	NP_001317301.1:n.-133-46dup
XM_017022208.1:c.-133-46dup	XP_016877697.1:n.-133-46dup
XM_017022209.2:c.-7+303dup	XP_016877698.1:n.-7+303dup
NM_002435.3:c.17-135dup MANE Select	NP_002426.1:n.17-135dup
NM_001289155.2:c.17-135dup	NP_001276084.1:n.17-135dup
NM_001289156.2:c.-7+303dup	NP_001276085.1:n.-7+303dup
NM_001289157.2:c.17-135dup	NP_001276086.1:n.17-135dup
NM_001330372.2:c.-133-46dup	NP_001317301.1:n.-133-46dup