Canonical Allele Identifier: CA491491449

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188638C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896297C>T , CM000677.2:g.74896297C>T	GRCh38
NC_000015.9:g.75188638C>T , CM000677.1:g.75188638C>T	GRCh37
NC_000015.8:g.72975691C>T	NCBI36
NG_008921.1:g.11229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.816C>T MANE Select	ENSP00000318318.6:p.Ala272=
ENST00000323744.10:c.633C>T	ENSP00000318192.6:p.Ala211=
ENST00000352410.8:c.816C>T	ENSP00000318318.6:p.Ala272=
ENST00000535694.5:c.666C>T	ENSP00000440447.1:p.Ala222=
ENST00000562606.5:c.756C>T	ENSP00000457020.1:p.Ala252=
ENST00000562800.5:c.256-1242C>T	ENSP00000457619.1:n.256-1242C>T
ENST00000563422.5:c.816C>T	ENSP00000457885.1:p.Ala272=
ENST00000563786.5:c.756C>T	ENSP00000455241.1:p.Ala252=
ENST00000564003.5:c.483C>T	ENSP00000454312.1:p.Ala161=
ENST00000566377.5:c.816C>T	ENSP00000455405.1:p.Ala272=
ENST00000566556.1:n.864C>T
ENST00000567177.1:c.594C>T	ENSP00000457013.1:p.Ala198=
ENST00000569931.5:c.756C>T	ENSP00000455161.1:p.Ala252=
NM_001289155.1:c.816C>T	NP_001276084.1:p.Ala272=
NM_001289156.1:c.666C>T	NP_001276085.1:p.Ala222=
NM_001289157.1:c.633C>T	NP_001276086.1:p.Ala211=
NM_002435.2:c.816C>T	NP_002426.1:p.Ala272=
XM_011521592.1:c.804C>T	XP_011519894.1:p.Ala268=
XM_011521593.1:c.756C>T	XP_011519895.1:p.Ala252=
NM_001330372.1:c.756C>T	NP_001317301.1:p.Ala252=
XM_017022208.1:c.756C>T	XP_016877697.1:p.Ala252=
XM_017022209.2:c.666C>T	XP_016877698.1:p.Ala222=
NM_002435.3:c.816C>T MANE Select	NP_002426.1:p.Ala272=
NM_001289155.2:c.816C>T	NP_001276084.1:p.Ala272=
NM_001289156.2:c.666C>T	NP_001276085.1:p.Ala222=
NM_001289157.2:c.633C>T	NP_001276086.1:p.Ala211=
NM_001330372.2:c.756C>T	NP_001317301.1:p.Ala252=