Canonical Allele Identifier: CA393176026

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188619A>C (hg19) ; chr15:g.74896278A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896278A>C , CM000677.2:g.74896278A>C	GRCh38
NC_000015.9:g.75188619A>C , CM000677.1:g.75188619A>C	GRCh37
NC_000015.8:g.72975672A>C	NCBI36
NG_008921.1:g.11210A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.797A>C MANE Select	ENSP00000318318.6:p.Glu266Ala
ENST00000323744.10:c.614A>C	ENSP00000318192.6:p.Glu205Ala
ENST00000352410.8:c.797A>C	ENSP00000318318.6:p.Glu266Ala
ENST00000535694.5:c.647A>C	ENSP00000440447.1:p.Glu216Ala
ENST00000562606.5:c.737A>C	ENSP00000457020.1:p.Glu246Ala
ENST00000562800.5:c.256-1261A>C	ENSP00000457619.1:n.256-1261A>C
ENST00000563422.5:c.797A>C	ENSP00000457885.1:p.Glu266Ala
ENST00000563786.5:c.737A>C	ENSP00000455241.1:p.Glu246Ala
ENST00000564003.5:c.464A>C	ENSP00000454312.1:p.Glu155Ala
ENST00000566377.5:c.797A>C	ENSP00000455405.1:p.Glu266Ala
ENST00000566556.1:n.845A>C
ENST00000567177.1:c.575A>C	ENSP00000457013.1:p.Glu192Ala
ENST00000569931.5:c.737A>C	ENSP00000455161.1:p.Glu246Ala
NM_001289155.1:c.797A>C	NP_001276084.1:p.Glu266Ala
NM_001289156.1:c.647A>C	NP_001276085.1:p.Glu216Ala
NM_001289157.1:c.614A>C	NP_001276086.1:p.Glu205Ala
NM_002435.2:c.797A>C	NP_002426.1:p.Glu266Ala
XM_011521592.1:c.785A>C	XP_011519894.1:p.Glu262Ala
XM_011521593.1:c.737A>C	XP_011519895.1:p.Glu246Ala
NM_001330372.1:c.737A>C	NP_001317301.1:p.Glu246Ala
XM_017022208.1:c.737A>C	XP_016877697.1:p.Glu246Ala
XM_017022209.2:c.647A>C	XP_016877698.1:p.Glu216Ala
NM_002435.3:c.797A>C MANE Select	NP_002426.1:p.Glu266Ala
NM_001289155.2:c.797A>C	NP_001276084.1:p.Glu266Ala
NM_001289156.2:c.647A>C	NP_001276085.1:p.Glu216Ala
NM_001289157.2:c.614A>C	NP_001276086.1:p.Glu205Ala
NM_001330372.2:c.737A>C	NP_001317301.1:p.Glu246Ala