Canonical Allele Identifier: CA491491375

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188524T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896183T>C , CM000677.2:g.74896183T>C	GRCh38
NC_000015.9:g.75188524T>C , CM000677.1:g.75188524T>C	GRCh37
NC_000015.8:g.72975577T>C	NCBI36
NG_008921.1:g.11115T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.702T>C MANE Select	ENSP00000318318.6:p.Phe234=
ENST00000323744.10:c.519T>C	ENSP00000318192.6:p.Phe173=
ENST00000352410.8:c.702T>C	ENSP00000318318.6:p.Phe234=
ENST00000535694.5:c.552T>C	ENSP00000440447.1:p.Phe184=
ENST00000561470.5:c.*598T>C	ENSP00000454267.1:n.*598T>C
ENST00000562606.5:c.642T>C	ENSP00000457020.1:p.Phe214=
ENST00000562800.5:c.256-1356T>C	ENSP00000457619.1:n.256-1356T>C
ENST00000563422.5:c.702T>C	ENSP00000457885.1:p.Phe234=
ENST00000563786.5:c.642T>C	ENSP00000455241.1:p.Phe214=
ENST00000564003.5:c.369T>C	ENSP00000454312.1:p.Phe123=
ENST00000566377.5:c.702T>C	ENSP00000455405.1:p.Phe234=
ENST00000566556.1:n.750T>C
ENST00000567177.1:c.480T>C	ENSP00000457013.1:p.Phe160=
ENST00000569931.5:c.642T>C	ENSP00000455161.1:p.Phe214=
NM_001289155.1:c.702T>C	NP_001276084.1:p.Phe234=
NM_001289156.1:c.552T>C	NP_001276085.1:p.Phe184=
NM_001289157.1:c.519T>C	NP_001276086.1:p.Phe173=
NM_002435.2:c.702T>C	NP_002426.1:p.Phe234=
XM_011521592.1:c.690T>C	XP_011519894.1:p.Phe230=
XM_011521593.1:c.642T>C	XP_011519895.1:p.Phe214=
NM_001330372.1:c.642T>C	NP_001317301.1:p.Phe214=
XM_017022208.1:c.642T>C	XP_016877697.1:p.Phe214=
XM_017022209.2:c.552T>C	XP_016877698.1:p.Phe184=
NM_002435.3:c.702T>C MANE Select	NP_002426.1:p.Phe234=
NM_001289155.2:c.702T>C	NP_001276084.1:p.Phe234=
NM_001289156.2:c.552T>C	NP_001276085.1:p.Phe184=
NM_001289157.2:c.519T>C	NP_001276086.1:p.Phe173=
NM_001330372.2:c.642T>C	NP_001317301.1:p.Phe214=