Canonical Allele Identifier: CA954128551
Gene: MIPEP HGNC NCBI

Linked Data

dbSNP Id: rs1870348285
gnomAD v3: 13-23862371-C-T
gnomAD v4: 13-23862371-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862371C>T , CM000675.2:g.23862371C>T GRCh38
NC_000013.10:g.24436510C>T , CM000675.1:g.24436510C>T GRCh37
NC_000013.9:g.23334510C>T NCBI36
NG_052977.1:g.32078G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.993-9G>A MANE Select ENSP00000371607.3:n.993-9G>A
ENST00000382172.3:c.993-9G>A ENSP00000371607.3:n.993-9G>A
ENST00000494139.1:n.390-9G>A
NM_005932.3:c.993-9G>A NP_005923.2:n.993-9G>A
XM_011535097.1:c.807-9G>A XP_011533399.1:n.807-9G>A
XM_011535098.1:c.993-9G>A XP_011533400.1:n.993-9G>A
XM_011535097.2:c.807-9G>A XP_011533399.1:n.807-9G>A
XM_011535098.3:c.993-9G>A XP_011533400.1:n.993-9G>A
NM_005932.4:c.993-9G>A MANE Select NP_005923.3:n.993-9G>A
Search 100 bp 5'
Search 100 bp 3'