Canonical Allele Identifier: CA971521411

Gene: MPI

Linked Data

• dbSNP Id: rs2064818389
• gnomAD v3: 15-74896356-GC-G
• gnomAD v4: 15-74896356-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896358del , CM000677.2:g.74896358del	GRCh38
NC_000015.9:g.75188699del , CM000677.1:g.75188699del	GRCh37
NC_000015.8:g.72975752del	NCBI36
NG_008921.1:g.11290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+33del MANE Select	ENSP00000318318.6:n.844+33del
ENST00000323744.10:c.661+33del	ENSP00000318192.6:n.661+33del
ENST00000352410.8:c.844+33del	ENSP00000318318.6:n.844+33del
ENST00000535694.5:c.694+33del	ENSP00000440447.1:n.694+33del
ENST00000562606.5:c.817del	ENSP00000457020.1:p.His273IlefsTer28
ENST00000562800.5:c.256-1181del	ENSP00000457619.1:n.256-1181del
ENST00000563422.5:c.877del	ENSP00000457885.1:p.His293IlefsTer28
ENST00000563786.5:c.784+33del	ENSP00000455241.1:n.784+33del
ENST00000564003.5:c.544del	ENSP00000454312.1:p.His182IlefsTer28
ENST00000566377.5:c.844+33del	ENSP00000455405.1:n.844+33del
ENST00000566556.1:n.925del
ENST00000567177.1:c.622+33del	ENSP00000457013.1:n.622+33del
ENST00000569931.5:c.784+33del	ENSP00000455161.1:n.784+33del
NM_001289155.1:c.844+33del	NP_001276084.1:n.844+33del
NM_001289156.1:c.694+33del	NP_001276085.1:n.694+33del
NM_001289157.1:c.661+33del	NP_001276086.1:n.661+33del
NM_002435.2:c.844+33del	NP_002426.1:n.844+33del
XM_011521592.1:c.832+33del	XP_011519894.1:n.832+33del
XM_011521593.1:c.784+33del	XP_011519895.1:n.784+33del
NM_001330372.1:c.784+33del	NP_001317301.1:n.784+33del
XM_017022208.1:c.784+33del	XP_016877697.1:n.784+33del
XM_017022209.2:c.694+33del	XP_016877698.1:n.694+33del
NM_002435.3:c.844+33del MANE Select	NP_002426.1:n.844+33del
NM_001289155.2:c.844+33del	NP_001276084.1:n.844+33del
NM_001289156.2:c.694+33del	NP_001276085.1:n.694+33del
NM_001289157.2:c.661+33del	NP_001276086.1:n.661+33del
NM_001330372.2:c.784+33del	NP_001317301.1:n.784+33del