Canonical Allele Identifier: CA2610032589

Gene: MINPP1

Linked Data

• gnomAD v4: 10-87508416-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508423del , CM000672.2:g.87508423del	GRCh38
NC_000010.10:g.89268180del , CM000672.1:g.89268180del	GRCh37
NC_000010.9:g.89258160del	NCBI36
NG_013023.1:g.8958del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.725del MANE Select	ENSP00000361064.4:p.Asn242MetfsTer21
ENST00000371994.8:c.725del	ENSP00000361062.4:p.Asn242MetfsTer21
ENST00000371996.8:c.725del	ENSP00000361064.4:p.Asn242MetfsTer21
ENST00000536010.1:c.122del	ENSP00000437823.1:p.Asn41MetfsTer21
NM_001178117.1:c.725del	NP_001171588.1:p.Asn242MetfsTer21
NM_001178118.1:c.122del	NP_001171589.1:p.Asn41MetfsTer21
NM_004897.4:c.725del	NP_004888.2:p.Asn242MetfsTer21
XM_006718078.2:c.725del	XP_006718141.1:p.Asn242MetfsTer21
XM_011540379.1:c.122del	XP_011538681.1:p.Asn41MetfsTer21
XR_945884.1:n.2849del
XM_006718078.3:c.725del	XP_006718141.1:p.Asn242MetfsTer21
XM_011540379.3:c.122del	XP_011538681.1:p.Asn41MetfsTer21
XM_017016965.2:c.725del	XP_016872454.1:p.Asn242MetfsTer21
NM_004897.5:c.725del MANE Select	NP_004888.2:p.Asn242MetfsTer21
NM_001178117.2:c.725del	NP_001171588.1:p.Asn242MetfsTer21
NM_001178118.2:c.122del	NP_001171589.1:p.Asn41MetfsTer21