Canonical Allele Identifier: CA147581

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74893329A>G , CM000677.2:g.74893329A>G	GRCh38
NC_000015.9:g.75185670A>G , CM000677.1:g.75185670A>G	GRCh37
NC_000015.8:g.72972723A>G	NCBI36
NG_008921.1:g.8261A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002435.3:c.670+9A>G MANE Select	NP_002426.1:n.670+9A>G
ENST00000352410.9:c.670+9A>G MANE Select	ENSP00000318318.6:n.670+9A>G
NM_001289155.1:c.670+9A>G	NP_001276084.1:n.670+9A>G
NM_001289155.2:c.670+9A>G	NP_001276084.1:n.670+9A>G
NM_001289156.1:c.520+9A>G	NP_001276085.1:n.520+9A>G
NM_001289156.2:c.520+9A>G	NP_001276085.1:n.520+9A>G
NM_001289157.1:c.487+527A>G	NP_001276086.1:n.487+527A>G
NM_001289157.2:c.487+527A>G	NP_001276086.1:n.487+527A>G
NM_001330372.1:c.610+9A>G	NP_001317301.1:n.610+9A>G
NM_001330372.2:c.610+9A>G	NP_001317301.1:n.610+9A>G
NM_002435.2:c.670+9A>G	NP_002426.1:n.670+9A>G
ENST00000323744.10:c.487+527A>G	ENSP00000318192.6:n.487+527A>G
ENST00000352410.8:c.670+9A>G	ENSP00000318318.6:n.670+9A>G
ENST00000535694.5:c.520+9A>G	ENSP00000440447.1:n.520+9A>G
ENST00000561470.5:c.*566+9A>G	ENSP00000454267.1:n.*566+9A>G
ENST00000562606.5:c.610+9A>G	ENSP00000457020.1:n.610+9A>G
ENST00000562800.5:c.255+1840A>G	ENSP00000457619.1:n.255+1840A>G
ENST00000563422.5:c.670+9A>G	ENSP00000457885.1:n.670+9A>G
ENST00000563786.5:c.610+9A>G	ENSP00000455241.1:n.610+9A>G
ENST00000564003.5:c.337+527A>G	ENSP00000454312.1:n.337+527A>G
ENST00000565576.5:c.679A>G	ENSP00000454619.1:p.Ser227Gly
ENST00000566377.5:c.670+9A>G	ENSP00000455405.1:n.670+9A>G
ENST00000567177.1:c.448+527A>G	ENSP00000457013.1:n.448+527A>G
ENST00000569931.5:c.610+9A>G	ENSP00000455161.1:n.610+9A>G
XM_011521592.1:c.658+9A>G	XP_011519894.1:n.658+9A>G
XM_011521593.1:c.610+9A>G	XP_011519895.1:n.610+9A>G
XM_017022208.1:c.610+9A>G	XP_016877697.1:n.610+9A>G
XM_017022209.2:c.520+9A>G	XP_016877698.1:n.520+9A>G