Canonical Allele Identifier: CA393174491

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75185555G>T (hg19) ; chr15:g.74893214G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74893214G>T , CM000677.2:g.74893214G>T	GRCh38
NC_000015.9:g.75185555G>T , CM000677.1:g.75185555G>T	GRCh37
NC_000015.8:g.72972608G>T	NCBI36
NG_008921.1:g.8146G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.564G>T MANE Select	ENSP00000318318.6:p.Gln188His
ENST00000323744.10:c.487+412G>T	ENSP00000318192.6:n.487+412G>T
ENST00000352410.8:c.564G>T	ENSP00000318318.6:p.Gln188His
ENST00000535694.5:c.414G>T	ENSP00000440447.1:p.Gln138His
ENST00000561470.5:c.*460G>T	ENSP00000454267.1:n.*460G>T
ENST00000562606.5:c.504G>T	ENSP00000457020.1:p.Gln168His
ENST00000562800.5:c.255+1725G>T	ENSP00000457619.1:n.255+1725G>T
ENST00000563422.5:c.564G>T	ENSP00000457885.1:p.Gln188His
ENST00000563786.5:c.504G>T	ENSP00000455241.1:p.Gln168His
ENST00000564003.5:c.337+412G>T	ENSP00000454312.1:n.337+412G>T
ENST00000564633.5:c.504G>T	ENSP00000455383.1:p.Gln168His
ENST00000565576.5:c.564G>T	ENSP00000454619.1:p.Gln188His
ENST00000566377.5:c.564G>T	ENSP00000455405.1:p.Gln188His
ENST00000567132.5:c.522G>T	ENSP00000455972.1:p.Gln174His
ENST00000567177.1:c.448+412G>T	ENSP00000457013.1:n.448+412G>T
ENST00000568828.5:c.528G>T	ENSP00000455065.1:p.Gln176His
ENST00000568907.5:c.474G>T	ENSP00000457494.1:p.Gln158His
ENST00000569931.5:c.504G>T	ENSP00000455161.1:p.Gln168His
NM_001289155.1:c.564G>T	NP_001276084.1:p.Gln188His
NM_001289156.1:c.414G>T	NP_001276085.1:p.Gln138His
NM_001289157.1:c.487+412G>T	NP_001276086.1:n.487+412G>T
NM_002435.2:c.564G>T	NP_002426.1:p.Gln188His
XM_011521592.1:c.552G>T	XP_011519894.1:p.Gln184His
XM_011521593.1:c.504G>T	XP_011519895.1:p.Gln168His
NM_001330372.1:c.504G>T	NP_001317301.1:p.Gln168His
XM_017022208.1:c.504G>T	XP_016877697.1:p.Gln168His
XM_017022209.2:c.414G>T	XP_016877698.1:p.Gln138His
NM_002435.3:c.564G>T MANE Select	NP_002426.1:p.Gln188His
NM_001289155.2:c.564G>T	NP_001276084.1:p.Gln188His
NM_001289156.2:c.414G>T	NP_001276085.1:p.Gln138His
NM_001289157.2:c.487+412G>T	NP_001276086.1:n.487+412G>T
NM_001330372.2:c.504G>T	NP_001317301.1:p.Gln168His