Canonical Allele Identifier: CA2187896823
Community Standard Title: NM_002435.3(MPI):c.413T= (p.Met138=)
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74892728T= , CM000677.2:g.74892728T= GRCh38
NC_000015.9:g.75185069T= , CM000677.1:g.75185069T= GRCh37
NC_000015.8:g.72972122T= NCBI36
NG_008921.1:g.7660T=

Transcript Alleles

HGVS Amino-acid Change
NM_002435.3:c.413T= MANE Select NP_002426.1:p.Met138=
ENST00000352410.9:c.413T= MANE Select ENSP00000318318.6:p.Met138=
NM_001289155.1:c.413T= NP_001276084.1:p.Met138=
NM_001289155.2:c.413T= NP_001276084.1:p.Met138=
NM_001289156.1:c.263T= NP_001276085.1:p.Met88=
NM_001289156.2:c.263T= NP_001276085.1:p.Met88=
NM_001289157.1:c.413T= NP_001276086.1:p.Met138=
NM_001289157.2:c.413T= NP_001276086.1:p.Met138=
NM_001330372.1:c.353T= NP_001317301.1:p.Met118=
NM_001330372.2:c.353T= NP_001317301.1:p.Met118=
NM_002435.2:c.413T= NP_002426.1:p.Met138=
ENST00000323744.10:c.413T= ENSP00000318192.6:p.Met138=
ENST00000352410.8:c.413T= ENSP00000318318.6:p.Met138=
ENST00000535694.5:c.263T= ENSP00000440447.1:p.Met88=
ENST00000561470.5:c.*309T= ENSP00000454267.1:n.*309T=
ENST00000562606.5:c.353T= ENSP00000457020.1:p.Met118=
ENST00000562800.5:c.255+1239T= ENSP00000457619.1:n.255+1239T=
ENST00000563422.5:c.413T= ENSP00000457885.1:p.Met138=
ENST00000563786.5:c.353T= ENSP00000455241.1:p.Met118=
ENST00000564003.5:c.263T= ENSP00000454312.1:p.Met88=
ENST00000564633.5:c.353T= ENSP00000455383.1:p.Met118=
ENST00000565576.5:c.413T= ENSP00000454619.1:p.Met138=
ENST00000566377.5:c.413T= ENSP00000455405.1:p.Met138=
ENST00000567116.5:n.444T=
ENST00000567132.5:c.371T= ENSP00000455972.1:p.Met124=
ENST00000567177.1:c.374T= ENSP00000457013.1:p.Met125=
ENST00000567570.5:c.353T= ENSP00000455477.1:p.Met118=
ENST00000568828.5:c.377T= ENSP00000455065.1:p.Met126=
ENST00000568840.1:n.522T=
ENST00000568907.5:c.323T= ENSP00000457494.1:p.Met108=
ENST00000569233.5:c.470T= ENSP00000454622.1:p.Met157=
ENST00000569931.5:c.353T= ENSP00000455161.1:p.Met118=
XM_011521592.1:c.401T= XP_011519894.1:p.Met134=
XM_011521593.1:c.353T= XP_011519895.1:p.Met118=
XM_017022208.1:c.353T= XP_016877697.1:p.Met118=
XM_017022209.2:c.263T= XP_016877698.1:p.Met88=