Canonical Allele Identifier: CA2622340323
Gene: MIPEP HGNC NCBI

Linked Data

gnomAD v4: 13-23862275-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862275A>T , CM000675.2:g.23862275A>T GRCh38
NC_000013.10:g.24436414A>T , CM000675.1:g.24436414A>T GRCh37
NC_000013.9:g.23334414A>T NCBI36
NG_052977.1:g.32174T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1053+27T>A MANE Select ENSP00000371607.3:n.1053+27T>A
ENST00000382172.3:c.1053+27T>A ENSP00000371607.3:n.1053+27T>A
ENST00000494139.1:n.450+27T>A
NM_005932.3:c.1053+27T>A NP_005923.2:n.1053+27T>A
XM_011535097.1:c.867+27T>A XP_011533399.1:n.867+27T>A
XM_011535098.1:c.1053+27T>A XP_011533400.1:n.1053+27T>A
XM_011535097.2:c.867+27T>A XP_011533399.1:n.867+27T>A
XM_011535098.3:c.1053+27T>A XP_011533400.1:n.1053+27T>A
NM_005932.4:c.1053+27T>A MANE Select NP_005923.3:n.1053+27T>A
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