Canonical Allele Identifier: CA2629527434
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74890522_74890535dup , CM000677.2:g.74890522_74890535dup GRCh38
NC_000015.9:g.75182863_75182876dup , CM000677.1:g.75182863_75182876dup GRCh37
NC_000015.8:g.72969916_72969929dup NCBI36
NG_008921.1:g.5454_5467dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.17-5_25dup
ENST00000323744.10:c.17-5_25dup
ENST00000352410.8:c.17-5_25dup
ENST00000535694.5:c.-7+433_-7+446dup ENSP00000440447.1:n.-7+433_-7+446dup
ENST00000561470.5:c.129-5_137dup
ENST00000562606.5:c.-18-31_-18-18dup ENSP00000457020.1:n.-18-31_-18-18dup
ENST00000562800.5:c.17-5_25dup
ENST00000563422.5:c.17-5_25dup
ENST00000563786.5:c.-49_-36dup ENSP00000455241.1:n.-49_-36dup
ENST00000564003.5:c.-7+433_-7+446dup ENSP00000454312.1:n.-7+433_-7+446dup
ENST00000564633.5:c.-15-34_-15-21dup ENSP00000455383.1:n.-15-34_-15-21dup
ENST00000565576.5:c.17-5_25dup
ENST00000566377.5:c.17-5_25dup
ENST00000567116.5:n.48-5_56dup
ENST00000567132.5:c.17-5_25dup
ENST00000567570.5:c.-49_-36dup ENSP00000455477.1:n.-49_-36dup
ENST00000568303.1:n.129_142dup
ENST00000568828.5:c.17-5_25dup
ENST00000568840.1:n.126-5_134dup
ENST00000568907.5:c.17-5_25dup
ENST00000569233.5:c.17-5_25dup
ENST00000569931.5:c.-18-31_-18-18dup ENSP00000455161.1:n.-18-31_-18-18dup
NM_001289155.1:c.17-5_25dup
NM_001289156.1:c.-7+433_-7+446dup NP_001276085.1:n.-7+433_-7+446dup
NM_001289157.1:c.17-5_25dup
NM_002435.2:c.17-5_25dup
XM_011521592.1:c.5-5_13dup
XM_011521593.1:c.-49_-36dup XP_011519895.1:n.-49_-36dup
NM_001330372.1:c.-49_-36dup NP_001317301.1:n.-49_-36dup
XM_017022208.1:c.-49_-36dup XP_016877697.1:n.-49_-36dup
XM_017022209.2:c.-7+433_-7+446dup XP_016877698.1:n.-7+433_-7+446dup
NM_002435.3:c.17-5_25dup
NM_001289155.2:c.17-5_25dup
NM_001289156.2:c.-7+433_-7+446dup NP_001276085.1:n.-7+433_-7+446dup
NM_001289157.2:c.17-5_25dup
NM_001330372.2:c.-49_-36dup NP_001317301.1:n.-49_-36dup