Canonical Allele Identifier: CA387526235
Gene: MIPEP HGNC NCBI

Linked Data

gnomAD v4: 13-23862363-C-T
MyVariant Identifiers: chr13:g.24436502C>T (hg19) chr13:g.23862363C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23862363C>T , CM000675.2:g.23862363C>T GRCh38
NC_000013.10:g.24436502C>T , CM000675.1:g.24436502C>T GRCh37
NC_000013.9:g.23334502C>T NCBI36
NG_052977.1:g.32086G>A

Transcript Alleles

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