Canonical Allele Identifier: CA2575370339
Gene: MIPEP HGNC NCBI

Linked Data

gnomAD v4: 13-23862403-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862403T>C , CM000675.2:g.23862403T>C GRCh38
NC_000013.10:g.24436542T>C , CM000675.1:g.24436542T>C GRCh37
NC_000013.9:g.23334542T>C NCBI36
NG_052977.1:g.32046A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.993-41A>G MANE Select ENSP00000371607.3:n.993-41A>G
ENST00000382172.3:c.993-41A>G ENSP00000371607.3:n.993-41A>G
ENST00000494139.1:n.390-41A>G
NM_005932.3:c.993-41A>G NP_005923.2:n.993-41A>G
XM_011535097.1:c.807-41A>G XP_011533399.1:n.807-41A>G
XM_011535098.1:c.993-41A>G XP_011533400.1:n.993-41A>G
XM_011535097.2:c.807-41A>G XP_011533399.1:n.807-41A>G
XM_011535098.3:c.993-41A>G XP_011533400.1:n.993-41A>G
NM_005932.4:c.993-41A>G MANE Select NP_005923.3:n.993-41A>G
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