Canonical Allele Identifier: CA491491423

Gene: MPI

Linked Data

• ClinVar Variation Id: 1554159
• ClinVar RCV Id: RCV002190026
• dbSNP Id: rs2141206797
• MyVariant Identifiers: chr15:g.75188605C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896264C>A , CM000677.2:g.74896264C>A	GRCh38
NC_000015.9:g.75188605C>A , CM000677.1:g.75188605C>A	GRCh37
NC_000015.8:g.72975658C>A	NCBI36
NG_008921.1:g.11196C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.783C>A MANE Select	ENSP00000318318.6:p.Thr261=
ENST00000323744.10:c.600C>A	ENSP00000318192.6:p.Thr200=
ENST00000352410.8:c.783C>A	ENSP00000318318.6:p.Thr261=
ENST00000535694.5:c.633C>A	ENSP00000440447.1:p.Thr211=
ENST00000562606.5:c.723C>A	ENSP00000457020.1:p.Thr241=
ENST00000562800.5:c.256-1275C>A	ENSP00000457619.1:n.256-1275C>A
ENST00000563422.5:c.783C>A	ENSP00000457885.1:p.Thr261=
ENST00000563786.5:c.723C>A	ENSP00000455241.1:p.Thr241=
ENST00000564003.5:c.450C>A	ENSP00000454312.1:p.Thr150=
ENST00000566377.5:c.783C>A	ENSP00000455405.1:p.Thr261=
ENST00000566556.1:n.831C>A
ENST00000567177.1:c.561C>A	ENSP00000457013.1:p.Thr187=
ENST00000569931.5:c.723C>A	ENSP00000455161.1:p.Thr241=
NM_001289155.1:c.783C>A	NP_001276084.1:p.Thr261=
NM_001289156.1:c.633C>A	NP_001276085.1:p.Thr211=
NM_001289157.1:c.600C>A	NP_001276086.1:p.Thr200=
NM_002435.2:c.783C>A	NP_002426.1:p.Thr261=
XM_011521592.1:c.771C>A	XP_011519894.1:p.Thr257=
XM_011521593.1:c.723C>A	XP_011519895.1:p.Thr241=
NM_001330372.1:c.723C>A	NP_001317301.1:p.Thr241=
XM_017022208.1:c.723C>A	XP_016877697.1:p.Thr241=
XM_017022209.2:c.633C>A	XP_016877698.1:p.Thr211=
NM_002435.3:c.783C>A MANE Select	NP_002426.1:p.Thr261=
NM_001289155.2:c.783C>A	NP_001276084.1:p.Thr261=
NM_001289156.2:c.633C>A	NP_001276085.1:p.Thr211=
NM_001289157.2:c.600C>A	NP_001276086.1:p.Thr200=
NM_001330372.2:c.723C>A	NP_001317301.1:p.Thr241=