Canonical Allele Identifier: CA393168856
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74890530T>C , CM000677.2:g.74890530T>C GRCh38
NC_000015.9:g.75182871T>C , CM000677.1:g.75182871T>C GRCh37
NC_000015.8:g.72969924T>C NCBI36
NG_008921.1:g.5462T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.20T>C MANE Select ENSP00000318318.6:p.Phe7Ser
ENST00000323744.10:c.20T>C ENSP00000318192.6:p.Phe7Ser
ENST00000352410.8:c.20T>C ENSP00000318318.6:p.Phe7Ser
ENST00000535694.5:c.-7+441T>C ENSP00000440447.1:n.-7+441T>C
ENST00000561470.5:c.132T>C ENSP00000454267.1:p.Ile44=
ENST00000562606.5:c.-18-23T>C ENSP00000457020.1:n.-18-23T>C
ENST00000562800.5:c.20T>C ENSP00000457619.1:p.Phe7Ser
ENST00000563422.5:c.20T>C ENSP00000457885.1:p.Phe7Ser
ENST00000563786.5:c.-41T>C ENSP00000455241.1:n.-41T>C
ENST00000564003.5:c.-7+441T>C ENSP00000454312.1:n.-7+441T>C
ENST00000564633.5:c.-15-26T>C ENSP00000455383.1:n.-15-26T>C
ENST00000565576.5:c.20T>C ENSP00000454619.1:p.Phe7Ser
ENST00000566377.5:c.20T>C ENSP00000455405.1:p.Phe7Ser
ENST00000567116.5:n.51T>C
ENST00000567132.5:c.20T>C ENSP00000455972.1:p.Phe7Ser
ENST00000567570.5:c.-41T>C ENSP00000455477.1:n.-41T>C
ENST00000568303.1:n.137T>C
ENST00000568828.5:c.20T>C ENSP00000455065.1:p.Phe7Ser
ENST00000568840.1:n.129T>C
ENST00000568907.5:c.20T>C ENSP00000457494.1:p.Phe7Ser
ENST00000569233.5:c.20T>C ENSP00000454622.1:p.Phe7Ser
ENST00000569931.5:c.-18-23T>C ENSP00000455161.1:n.-18-23T>C
NM_001289155.1:c.20T>C NP_001276084.1:p.Phe7Ser
NM_001289156.1:c.-7+441T>C NP_001276085.1:n.-7+441T>C
NM_001289157.1:c.20T>C NP_001276086.1:p.Phe7Ser
NM_002435.2:c.20T>C NP_002426.1:p.Phe7Ser
XM_011521592.1:c.8T>C XP_011519894.1:p.Phe3Ser
XM_011521593.1:c.-41T>C XP_011519895.1:n.-41T>C
NM_001330372.1:c.-41T>C NP_001317301.1:n.-41T>C
XM_017022208.1:c.-41T>C XP_016877697.1:n.-41T>C
XM_017022209.2:c.-7+441T>C XP_016877698.1:n.-7+441T>C
NM_002435.3:c.20T>C MANE Select NP_002426.1:p.Phe7Ser
NM_001289155.2:c.20T>C NP_001276084.1:p.Phe7Ser
NM_001289156.2:c.-7+441T>C NP_001276085.1:n.-7+441T>C
NM_001289157.2:c.20T>C NP_001276086.1:p.Phe7Ser
NM_001330372.2:c.-41T>C NP_001317301.1:n.-41T>C