Canonical Allele Identifier: CA393176098

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188652C>T (hg19) ; chr15:g.74896311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896311C>T , CM000677.2:g.74896311C>T	GRCh38
NC_000015.9:g.75188652C>T , CM000677.1:g.75188652C>T	GRCh37
NC_000015.8:g.72975705C>T	NCBI36
NG_008921.1:g.11243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.830C>T MANE Select	ENSP00000318318.6:p.Ala277Val
ENST00000323744.10:c.647C>T	ENSP00000318192.6:p.Ala216Val
ENST00000352410.8:c.830C>T	ENSP00000318318.6:p.Ala277Val
ENST00000535694.5:c.680C>T	ENSP00000440447.1:p.Ala227Val
ENST00000562606.5:c.770C>T	ENSP00000457020.1:p.Ala257Val
ENST00000562800.5:c.256-1228C>T	ENSP00000457619.1:n.256-1228C>T
ENST00000563422.5:c.830C>T	ENSP00000457885.1:p.Ala277Val
ENST00000563786.5:c.770C>T	ENSP00000455241.1:p.Ala257Val
ENST00000564003.5:c.497C>T	ENSP00000454312.1:p.Ala166Val
ENST00000566377.5:c.830C>T	ENSP00000455405.1:p.Ala277Val
ENST00000566556.1:n.878C>T
ENST00000567177.1:c.608C>T	ENSP00000457013.1:p.Ala203Val
ENST00000569931.5:c.770C>T	ENSP00000455161.1:p.Ala257Val
NM_001289155.1:c.830C>T	NP_001276084.1:p.Ala277Val
NM_001289156.1:c.680C>T	NP_001276085.1:p.Ala227Val
NM_001289157.1:c.647C>T	NP_001276086.1:p.Ala216Val
NM_002435.2:c.830C>T	NP_002426.1:p.Ala277Val
XM_011521592.1:c.818C>T	XP_011519894.1:p.Ala273Val
XM_011521593.1:c.770C>T	XP_011519895.1:p.Ala257Val
NM_001330372.1:c.770C>T	NP_001317301.1:p.Ala257Val
XM_017022208.1:c.770C>T	XP_016877697.1:p.Ala257Val
XM_017022209.2:c.680C>T	XP_016877698.1:p.Ala227Val
NM_002435.3:c.830C>T MANE Select	NP_002426.1:p.Ala277Val
NM_001289155.2:c.830C>T	NP_001276084.1:p.Ala277Val
NM_001289156.2:c.680C>T	NP_001276085.1:p.Ala227Val
NM_001289157.2:c.647C>T	NP_001276086.1:p.Ala216Val
NM_001330372.2:c.770C>T	NP_001317301.1:p.Ala257Val