Canonical Allele Identifier: CA6913139
Gene: MIPEP HGNC NCBI

Linked Data

dbSNP Id: rs770388174
ExAC: 13:24436457 A / C
gnomAD v2: 13-24436457-A-C
gnomAD v3: 13-23862318-A-C
gnomAD v4: 13-23862318-A-C
MyVariant Identifiers: chr13:g.24436457A>C (hg19) chr13:g.23862318A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862318A>C , CM000675.2:g.23862318A>C GRCh38
NC_000013.10:g.24436457A>C , CM000675.1:g.24436457A>C GRCh37
NC_000013.9:g.23334457A>C NCBI36
NG_052977.1:g.32131T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382172.4:c.1037T>G MANE Select ENSP00000371607.3:p.Leu346Arg
ENST00000382172.3:c.1037T>G ENSP00000371607.3:p.Leu346Arg
ENST00000494139.1:n.434T>G
NM_005932.3:c.1037T>G NP_005923.2:p.Leu346Arg
XM_011535097.1:c.851T>G XP_011533399.1:p.Leu284Arg
XM_011535098.1:c.1037T>G XP_011533400.1:p.Leu346Arg
XM_011535097.2:c.851T>G XP_011533399.1:p.Leu284Arg
XM_011535098.3:c.1037T>G XP_011533400.1:p.Leu346Arg
NM_005932.4:c.1037T>G MANE Select NP_005923.3:p.Leu346Arg
Search 100 bp 5'
Search 100 bp 3'