Canonical Allele Identifier: CA7662580

Gene: MPI

Linked Data

• ClinVar Variation Id: 2897769
• ClinVar RCV Id: RCV003629642
• dbSNP Id: rs760199403
• ExAC: 15:75189334 TGAC / T
• gnomAD v2: 15-75189334-TGAC-T
• gnomAD v3: 15-74896993-TGAC-T
• gnomAD v4: 15-74896993-TGAC-T
• MyVariant Identifiers: chr15:g.75189335_75189337del (hg19) ; chr15:g.74896994_74896996del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896997_74896999del , CM000677.2:g.74896997_74896999del	GRCh38
NC_000015.9:g.75189338_75189340del , CM000677.1:g.75189338_75189340del	GRCh37
NC_000015.8:g.72976391_72976393del	NCBI36
NG_008921.1:g.11929_11931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.845-14_845-12del MANE Select	ENSP00000318318.6:n.845-14_845-12del
ENST00000323744.10:c.662-14_662-12del	ENSP00000318192.6:n.662-14_662-12del
ENST00000352410.8:c.845-14_845-12del	ENSP00000318318.6:n.845-14_845-12del
ENST00000535694.5:c.695-14_695-12del	ENSP00000440447.1:n.695-14_695-12del
ENST00000562800.5:c.256-542_256-540del	ENSP00000457619.1:n.256-542_256-540del
ENST00000563786.5:c.785-14_785-12del	ENSP00000455241.1:n.785-14_785-12del
ENST00000566377.5:c.845-515_845-513del	ENSP00000455405.1:n.845-515_845-513del
ENST00000566556.1:n.1564_1566del
ENST00000567177.1:c.623-515_623-513del	ENSP00000457013.1:n.623-515_623-513del
ENST00000569931.5:c.785-14_785-12del	ENSP00000455161.1:n.785-14_785-12del
NM_001289155.1:c.845-515_845-513del	NP_001276084.1:n.845-515_845-513del
NM_001289156.1:c.695-14_695-12del	NP_001276085.1:n.695-14_695-12del
NM_001289157.1:c.662-14_662-12del	NP_001276086.1:n.662-14_662-12del
NM_002435.2:c.845-14_845-12del	NP_002426.1:n.845-14_845-12del
XM_011521592.1:c.833-14_833-12del	XP_011519894.1:n.833-14_833-12del
XM_011521593.1:c.785-14_785-12del	XP_011519895.1:n.785-14_785-12del
NM_001330372.1:c.785-14_785-12del	NP_001317301.1:n.785-14_785-12del
XM_017022208.1:c.785-515_785-513del	XP_016877697.1:n.785-515_785-513del
XM_017022209.2:c.695-515_695-513del	XP_016877698.1:n.695-515_695-513del
NM_002435.3:c.845-14_845-12del MANE Select	NP_002426.1:n.845-14_845-12del
NM_001289155.2:c.845-515_845-513del	NP_001276084.1:n.845-515_845-513del
NM_001289156.2:c.695-14_695-12del	NP_001276085.1:n.695-14_695-12del
NM_001289157.2:c.662-14_662-12del	NP_001276086.1:n.662-14_662-12del
NM_001330372.2:c.785-14_785-12del	NP_001317301.1:n.785-14_785-12del