Canonical Allele Identifier: CA2610032588
Gene: MINPP1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371996.9:c.725dup MANE Select ENSP00000361064.4:p.Asn242LysfsTer?
ENST00000371994.8:c.725dup ENSP00000361062.4:p.Asn242LysfsTer?
ENST00000371996.8:c.725dup ENSP00000361064.4:p.Asn242LysfsTer?
ENST00000536010.1:c.122dup ENSP00000437823.1:p.Asn41LysfsTer?
NM_001178117.1:c.725dup NP_001171588.1:p.Asn242LysfsTer?
NM_001178118.1:c.122dup NP_001171589.1:p.Asn41LysfsTer?
NM_004897.4:c.725dup NP_004888.2:p.Asn242LysfsTer?
XM_006718078.2:c.725dup XP_006718141.1:p.Asn242LysfsTer?
XM_011540379.1:c.122dup XP_011538681.1:p.Asn41LysfsTer?
XR_945884.1:n.2849dup
XM_006718078.3:c.725dup XP_006718141.1:p.Asn242LysfsTer?
XM_011540379.3:c.122dup XP_011538681.1:p.Asn41LysfsTer?
XM_017016965.2:c.725dup XP_016872454.1:p.Asn242LysfsTer?
NM_004897.5:c.725dup MANE Select NP_004888.2:p.Asn242LysfsTer?
NM_001178117.2:c.725dup NP_001171588.1:p.Asn242LysfsTer?
NM_001178118.2:c.122dup NP_001171589.1:p.Asn41LysfsTer?