Canonical Allele Identifier: CA2629527397

Gene: MPI

Linked Data

• gnomAD v4: 15-74890486-C-CTGAGGAGTGGAGTGGCAGCTGACCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890487_74890512dup , CM000677.2:g.74890487_74890512dup	GRCh38
NC_000015.9:g.75182828_75182853dup , CM000677.1:g.75182828_75182853dup	GRCh37
NC_000015.8:g.72969881_72969906dup	NCBI36
NG_008921.1:g.5419_5444dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.17-40_17-15dup MANE Select	ENSP00000318318.6:n.17-40_17-15dup
ENST00000323744.10:c.17-40_17-15dup	ENSP00000318192.6:n.17-40_17-15dup
ENST00000352410.8:c.17-40_17-15dup	ENSP00000318318.6:n.17-40_17-15dup
ENST00000535694.5:c.-7+398_-7+423dup	ENSP00000440447.1:n.-7+398_-7+423dup
ENST00000561470.5:c.129-40_129-15dup	ENSP00000454267.1:n.129-40_129-15dup
ENST00000562606.5:c.-18-66_-18-41dup	ENSP00000457020.1:n.-18-66_-18-41dup
ENST00000562800.5:c.17-40_17-15dup	ENSP00000457619.1:n.17-40_17-15dup
ENST00000563422.5:c.17-40_17-15dup	ENSP00000457885.1:n.17-40_17-15dup
ENST00000563786.5:c.-84_-59dup	ENSP00000455241.1:n.-84_-59dup
ENST00000564003.5:c.-7+398_-7+423dup	ENSP00000454312.1:n.-7+398_-7+423dup
ENST00000564633.5:c.-15-69_-15-44dup	ENSP00000455383.1:n.-15-69_-15-44dup
ENST00000565576.5:c.17-40_17-15dup	ENSP00000454619.1:n.17-40_17-15dup
ENST00000566377.5:c.17-40_17-15dup	ENSP00000455405.1:n.17-40_17-15dup
ENST00000567116.5:n.48-40_48-15dup
ENST00000567132.5:c.17-40_17-15dup	ENSP00000455972.1:n.17-40_17-15dup
ENST00000567570.5:c.-84_-59dup	ENSP00000455477.1:n.-84_-59dup
ENST00000568303.1:n.94_119dup
ENST00000568828.5:c.17-40_17-15dup	ENSP00000455065.1:n.17-40_17-15dup
ENST00000568840.1:n.126-40_126-15dup
ENST00000568907.5:c.17-40_17-15dup	ENSP00000457494.1:n.17-40_17-15dup
ENST00000569233.5:c.17-40_17-15dup	ENSP00000454622.1:n.17-40_17-15dup
ENST00000569931.5:c.-18-66_-18-41dup	ENSP00000455161.1:n.-18-66_-18-41dup
NM_001289155.1:c.17-40_17-15dup	NP_001276084.1:n.17-40_17-15dup
NM_001289156.1:c.-7+398_-7+423dup	NP_001276085.1:n.-7+398_-7+423dup
NM_001289157.1:c.17-40_17-15dup	NP_001276086.1:n.17-40_17-15dup
NM_002435.2:c.17-40_17-15dup	NP_002426.1:n.17-40_17-15dup
XM_011521592.1:c.5-40_5-15dup	XP_011519894.1:n.5-40_5-15dup
XM_011521593.1:c.-84_-59dup	XP_011519895.1:n.-84_-59dup
NM_001330372.1:c.-84_-59dup	NP_001317301.1:n.-84_-59dup
XM_017022208.1:c.-84_-59dup	XP_016877697.1:n.-84_-59dup
XM_017022209.2:c.-7+398_-7+423dup	XP_016877698.1:n.-7+398_-7+423dup
NM_002435.3:c.17-40_17-15dup MANE Select	NP_002426.1:n.17-40_17-15dup
NM_001289155.2:c.17-40_17-15dup	NP_001276084.1:n.17-40_17-15dup
NM_001289156.2:c.-7+398_-7+423dup	NP_001276085.1:n.-7+398_-7+423dup
NM_001289157.2:c.17-40_17-15dup	NP_001276086.1:n.17-40_17-15dup
NM_001330372.2:c.-84_-59dup	NP_001317301.1:n.-84_-59dup