Canonical Allele Identifier: CA393175965

Gene: MPI

Linked Data

• dbSNP Id: rs1442151213
• gnomAD v3: 15-74896248-T-C
• gnomAD v4: 15-74896248-T-C
• MyVariant Identifiers: chr15:g.75188589T>C (hg19) ; chr15:g.74896248T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896248T>C , CM000677.2:g.74896248T>C	GRCh38
NC_000015.9:g.75188589T>C , CM000677.1:g.75188589T>C	GRCh37
NC_000015.8:g.72975642T>C	NCBI36
NG_008921.1:g.11180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.767T>C MANE Select	ENSP00000318318.6:p.Phe256Ser
ENST00000323744.10:c.584T>C	ENSP00000318192.6:p.Phe195Ser
ENST00000352410.8:c.767T>C	ENSP00000318318.6:p.Phe256Ser
ENST00000535694.5:c.617T>C	ENSP00000440447.1:p.Phe206Ser
ENST00000562606.5:c.707T>C	ENSP00000457020.1:p.Phe236Ser
ENST00000562800.5:c.256-1291T>C	ENSP00000457619.1:n.256-1291T>C
ENST00000563422.5:c.767T>C	ENSP00000457885.1:p.Phe256Ser
ENST00000563786.5:c.707T>C	ENSP00000455241.1:p.Phe236Ser
ENST00000564003.5:c.434T>C	ENSP00000454312.1:p.Phe145Ser
ENST00000566377.5:c.767T>C	ENSP00000455405.1:p.Phe256Ser
ENST00000566556.1:n.815T>C
ENST00000567177.1:c.545T>C	ENSP00000457013.1:p.Phe182Ser
ENST00000569931.5:c.707T>C	ENSP00000455161.1:p.Phe236Ser
NM_001289155.1:c.767T>C	NP_001276084.1:p.Phe256Ser
NM_001289156.1:c.617T>C	NP_001276085.1:p.Phe206Ser
NM_001289157.1:c.584T>C	NP_001276086.1:p.Phe195Ser
NM_002435.2:c.767T>C	NP_002426.1:p.Phe256Ser
XM_011521592.1:c.755T>C	XP_011519894.1:p.Phe252Ser
XM_011521593.1:c.707T>C	XP_011519895.1:p.Phe236Ser
NM_001330372.1:c.707T>C	NP_001317301.1:p.Phe236Ser
XM_017022208.1:c.707T>C	XP_016877697.1:p.Phe236Ser
XM_017022209.2:c.617T>C	XP_016877698.1:p.Phe206Ser
NM_002435.3:c.767T>C MANE Select	NP_002426.1:p.Phe256Ser
NM_001289155.2:c.767T>C	NP_001276084.1:p.Phe256Ser
NM_001289156.2:c.617T>C	NP_001276085.1:p.Phe206Ser
NM_001289157.2:c.584T>C	NP_001276086.1:p.Phe195Ser
NM_001330372.2:c.707T>C	NP_001317301.1:p.Phe236Ser