Canonical Allele Identifier: CA2187897460
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74893313C= , CM000677.2:g.74893313C= GRCh38
NC_000015.9:g.75185654C= , CM000677.1:g.75185654C= GRCh37
NC_000015.8:g.72972707C= NCBI36
NG_008921.1:g.8245C=

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.663C= MANE Select ENSP00000318318.6:p.Ser221=
ENST00000323744.10:c.487+511C= ENSP00000318192.6:n.487+511C=
ENST00000352410.8:c.663C= ENSP00000318318.6:p.Ser221=
ENST00000535694.5:c.513C= ENSP00000440447.1:p.Ser171=
ENST00000561470.5:c.*559C= ENSP00000454267.1:n.*559C=
ENST00000562606.5:c.603C= ENSP00000457020.1:p.Ser201=
ENST00000562800.5:c.255+1824C= ENSP00000457619.1:n.255+1824C=
ENST00000563422.5:c.663C= ENSP00000457885.1:p.Ser221=
ENST00000563786.5:c.603C= ENSP00000455241.1:p.Ser201=
ENST00000564003.5:c.337+511C= ENSP00000454312.1:n.337+511C=
ENST00000565576.5:c.663C= ENSP00000454619.1:p.Ser221=
ENST00000566377.5:c.663C= ENSP00000455405.1:p.Ser221=
ENST00000567177.1:c.448+511C= ENSP00000457013.1:n.448+511C=
ENST00000569931.5:c.603C= ENSP00000455161.1:p.Ser201=
NM_001289155.1:c.663C= NP_001276084.1:p.Ser221=
NM_001289156.1:c.513C= NP_001276085.1:p.Ser171=
NM_001289157.1:c.487+511C= NP_001276086.1:n.487+511C=
NM_002435.2:c.663C= NP_002426.1:p.Ser221=
XM_011521592.1:c.651C= XP_011519894.1:p.Ser217=
XM_011521593.1:c.603C= XP_011519895.1:p.Ser201=
NM_001330372.1:c.603C= NP_001317301.1:p.Ser201=
XM_017022208.1:c.603C= XP_016877697.1:p.Ser201=
XM_017022209.2:c.513C= XP_016877698.1:p.Ser171=
NM_002435.3:c.663C= MANE Select NP_002426.1:p.Ser221=
NM_001289155.2:c.663C= NP_001276084.1:p.Ser221=
NM_001289156.2:c.513C= NP_001276085.1:p.Ser171=
NM_001289157.2:c.487+511C= NP_001276086.1:n.487+511C=
NM_001330372.2:c.603C= NP_001317301.1:p.Ser201=