Canonical Allele Identifier: CA2187902642

Gene: MPI

Linked Data

• dbSNP Id: rs2064827547

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896993T>C , CM000677.2:g.74896993T>C	GRCh38
NC_000015.9:g.75189334T>C , CM000677.1:g.75189334T>C	GRCh37
NC_000015.8:g.72976387T>C	NCBI36
NG_008921.1:g.11925T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.845-18T>C MANE Select	ENSP00000318318.6:n.845-18T>C
ENST00000323744.10:c.662-18T>C	ENSP00000318192.6:n.662-18T>C
ENST00000352410.8:c.845-18T>C	ENSP00000318318.6:n.845-18T>C
ENST00000535694.5:c.695-18T>C	ENSP00000440447.1:n.695-18T>C
ENST00000562800.5:c.256-546T>C	ENSP00000457619.1:n.256-546T>C
ENST00000563786.5:c.785-18T>C	ENSP00000455241.1:n.785-18T>C
ENST00000566377.5:c.845-519T>C	ENSP00000455405.1:n.845-519T>C
ENST00000566556.1:n.1560T>C
ENST00000567177.1:c.623-519T>C	ENSP00000457013.1:n.623-519T>C
ENST00000569931.5:c.785-18T>C	ENSP00000455161.1:n.785-18T>C
NM_001289155.1:c.845-519T>C	NP_001276084.1:n.845-519T>C
NM_001289156.1:c.695-18T>C	NP_001276085.1:n.695-18T>C
NM_001289157.1:c.662-18T>C	NP_001276086.1:n.662-18T>C
NM_002435.2:c.845-18T>C	NP_002426.1:n.845-18T>C
XM_011521592.1:c.833-18T>C	XP_011519894.1:n.833-18T>C
XM_011521593.1:c.785-18T>C	XP_011519895.1:n.785-18T>C
NM_001330372.1:c.785-18T>C	NP_001317301.1:n.785-18T>C
XM_017022208.1:c.785-519T>C	XP_016877697.1:n.785-519T>C
XM_017022209.2:c.695-519T>C	XP_016877698.1:n.695-519T>C
NM_002435.3:c.845-18T>C MANE Select	NP_002426.1:n.845-18T>C
NM_001289155.2:c.845-519T>C	NP_001276084.1:n.845-519T>C
NM_001289156.2:c.695-18T>C	NP_001276085.1:n.695-18T>C
NM_001289157.2:c.662-18T>C	NP_001276086.1:n.662-18T>C
NM_001330372.2:c.785-18T>C	NP_001317301.1:n.785-18T>C