Canonical Allele Identifier: CA387525993
Gene: MIPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.24436443A>C (hg19) chr13:g.23862304A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862304A>C , CM000675.2:g.23862304A>C GRCh38
NC_000013.10:g.24436443A>C , CM000675.1:g.24436443A>C GRCh37
NC_000013.9:g.23334443A>C NCBI36
NG_052977.1:g.32145T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1051T>G MANE Select ENSP00000371607.3:p.Ser351Ala
ENST00000382172.3:c.1051T>G ENSP00000371607.3:p.Ser351Ala
ENST00000494139.1:n.448T>G
NM_005932.3:c.1051T>G NP_005923.2:p.Ser351Ala
XM_011535097.1:c.865T>G XP_011533399.1:p.Ser289Ala
XM_011535098.1:c.1051T>G XP_011533400.1:p.Ser351Ala
XM_011535097.2:c.865T>G XP_011533399.1:p.Ser289Ala
XM_011535098.3:c.1051T>G XP_011533400.1:p.Ser351Ala
NM_005932.4:c.1051T>G MANE Select NP_005923.3:p.Ser351Ala
Search 100 bp 5'
Search 100 bp 3'