Canonical Allele Identifier: CA393175768

Gene: MPI

Linked Data

• dbSNP Id: rs727504018
• gnomAD v2: 15-75188499-C-A
• gnomAD v4: 15-74896158-C-A
• MyVariant Identifiers: chr15:g.75188499C>A (hg19) ; chr15:g.74896158C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896158C>A , CM000677.2:g.74896158C>A	GRCh38
NC_000015.9:g.75188499C>A , CM000677.1:g.75188499C>A	GRCh37
NC_000015.8:g.72975552C>A	NCBI36
NG_008921.1:g.11090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.677C>A MANE Select	ENSP00000318318.6:p.Ala226Asp
ENST00000323744.10:c.494C>A	ENSP00000318192.6:p.Ala165Asp
ENST00000352410.8:c.677C>A	ENSP00000318318.6:p.Ala226Asp
ENST00000535694.5:c.527C>A	ENSP00000440447.1:p.Ala176Asp
ENST00000561470.5:c.*573C>A	ENSP00000454267.1:n.*573C>A
ENST00000562606.5:c.617C>A	ENSP00000457020.1:p.Ala206Asp
ENST00000562800.5:c.256-1381C>A	ENSP00000457619.1:n.256-1381C>A
ENST00000563422.5:c.677C>A	ENSP00000457885.1:p.Ala226Asp
ENST00000563786.5:c.617C>A	ENSP00000455241.1:p.Ala206Asp
ENST00000564003.5:c.344C>A	ENSP00000454312.1:p.Ala115Asp
ENST00000566377.5:c.677C>A	ENSP00000455405.1:p.Ala226Asp
ENST00000566556.1:n.725C>A
ENST00000567177.1:c.455C>A	ENSP00000457013.1:p.Ala152Asp
ENST00000569931.5:c.617C>A	ENSP00000455161.1:p.Ala206Asp
NM_001289155.1:c.677C>A	NP_001276084.1:p.Ala226Asp
NM_001289156.1:c.527C>A	NP_001276085.1:p.Ala176Asp
NM_001289157.1:c.494C>A	NP_001276086.1:p.Ala165Asp
NM_002435.2:c.677C>A	NP_002426.1:p.Ala226Asp
XM_011521592.1:c.665C>A	XP_011519894.1:p.Ala222Asp
XM_011521593.1:c.617C>A	XP_011519895.1:p.Ala206Asp
NM_001330372.1:c.617C>A	NP_001317301.1:p.Ala206Asp
XM_017022208.1:c.617C>A	XP_016877697.1:p.Ala206Asp
XM_017022209.2:c.527C>A	XP_016877698.1:p.Ala176Asp
NM_002435.3:c.677C>A MANE Select	NP_002426.1:p.Ala226Asp
NM_001289155.2:c.677C>A	NP_001276084.1:p.Ala226Asp
NM_001289156.2:c.527C>A	NP_001276085.1:p.Ala176Asp
NM_001289157.2:c.494C>A	NP_001276086.1:p.Ala165Asp
NM_001330372.2:c.617C>A	NP_001317301.1:p.Ala206Asp