Canonical Allele Identifier: CA2658328565
Gene: MPV17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323095del , CM000664.2:g.27323095del GRCh38
NC_000002.11:g.27545962del , CM000664.1:g.27545962del GRCh37
NC_000002.10:g.27399466del NCBI36
NG_008075.1:g.4471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.-48del MANE Select ENSP00000369383.1:n.-48del
ENST00000357186.10:c.18+1339del ENSP00000349713.6:n.18+1339del
ENST00000380044.5:c.-48del ENSP00000369383.1:n.-48del
ENST00000399052.8:c.-48del ENSP00000382006.4:n.-48del
ENST00000405076.5:c.-48del ENSP00000385175.1:n.-48del
ENST00000486898.1:n.4del
ENST00000621183.4:n.9del
ENST00000621470.4:n.4del
NM_002437.4:c.-48del NP_002428.1:n.-48del
XM_005264327.2:c.-172del XP_005264384.1:n.-172del
XM_006712021.2:c.-253del XP_006712084.1:n.-253del
XM_006712021.3:c.-253del XP_006712084.1:n.-253del
XM_017004150.1:c.-3300del XP_016859639.1:n.-3300del
NM_002437.5:c.-48del MANE Select NP_002428.1:n.-48del