Canonical Allele Identifier: CA387526039
Gene: MIPEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862314A>C , CM000675.2:g.23862314A>C GRCh38
NC_000013.10:g.24436453A>C , CM000675.1:g.24436453A>C GRCh37
NC_000013.9:g.23334453A>C NCBI36
NG_052977.1:g.32135T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1041T>G MANE Select ENSP00000371607.3:p.Asn347Lys
ENST00000382172.3:c.1041T>G ENSP00000371607.3:p.Asn347Lys
ENST00000494139.1:n.438T>G
NM_005932.3:c.1041T>G NP_005923.2:p.Asn347Lys
XM_011535097.1:c.855T>G XP_011533399.1:p.Asn285Lys
XM_011535098.1:c.1041T>G XP_011533400.1:p.Asn347Lys
XM_011535097.2:c.855T>G XP_011533399.1:p.Asn285Lys
XM_011535098.3:c.1041T>G XP_011533400.1:p.Asn347Lys
NM_005932.4:c.1041T>G MANE Select NP_005923.3:p.Asn347Lys