Canonical Allele Identifier: CA2842319616
Gene: MPV17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27322544_27322545insACGGTGGG , CM000664.2:g.27322544_27322545insACGGTGGG GRCh38
NC_000002.11:g.27545411_27545412insACGGTGGG , CM000664.1:g.27545411_27545412insACGGTGGG GRCh37
NC_000002.10:g.27398915_27398916insACGGTGGG NCBI36
NG_008075.1:g.5023_5024insACCGTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.-5-20_-5-19insACCGTCCC MANE Select ENSP00000369383.1:n.-5-20_-5-19insACCGTCCC
ENST00000233545.6:c.-25_-24insACCGTCCC ENSP00000233545.2:n.-25_-24insACCGTCCC
ENST00000357186.10:c.18+1891_18+1892insACCGTCCC ENSP00000349713.6:n.18+1891_18+1892insACCGTCCC
ENST00000380044.5:c.-5-20_-5-19insACCGTCCC ENSP00000369383.1:n.-5-20_-5-19insACCGTCCC
ENST00000399052.8:c.-5-20_-5-19insACCGTCCC ENSP00000382006.4:n.-5-20_-5-19insACCGTCCC
ENST00000402310.5:c.-5-20_-5-19insACCGTCCC ENSP00000383955.1:n.-5-20_-5-19insACCGTCCC
ENST00000402722.5:c.-5-20_-5-19insACCGTCCC ENSP00000386000.1:n.-5-20_-5-19insACCGTCCC
ENST00000403262.6:c.-5-20_-5-19insACCGTCCC ENSP00000385671.1:n.-5-20_-5-19insACCGTCCC
ENST00000405076.5:c.-5-20_-5-19insACCGTCCC ENSP00000385175.1:n.-5-20_-5-19insACCGTCCC
ENST00000405983.5:c.-5-20_-5-19insACCGTCCC ENSP00000384586.1:n.-5-20_-5-19insACCGTCCC
ENST00000415514.5:c.-5-20_-5-19insACCGTCCC ENSP00000388043.1:n.-5-20_-5-19insACCGTCCC
ENST00000426513.6:c.-5-20_-5-19insACCGTCCC ENSP00000403824.2:n.-5-20_-5-19insACCGTCCC
ENST00000428910.5:c.-207-20_-207-19insACCGTCCC ENSP00000405235.1:n.-207-20_-207-19insACCGTCCC
ENST00000486898.1:n.47-20_47-19insACCGTCCC
ENST00000494436.1:n.27-20_27-19insACCGTCCC
ENST00000617583.4:n.22-20_22-19insACCGTCCC
ENST00000621183.4:n.52-20_52-19insACCGTCCC
ENST00000621470.4:n.47-20_47-19insACCGTCCC
ENST00000622003.4:n.12-20_12-19insACCGTCCC
NM_002437.4:c.-5-20_-5-19insACCGTCCC NP_002428.1:n.-5-20_-5-19insACCGTCCC
XM_005264326.2:c.-5-20_-5-19insACCGTCCC XP_005264383.1:n.-5-20_-5-19insACCGTCCC
XM_005264327.2:c.-129-20_-129-19insACCGTCCC XP_005264384.1:n.-129-20_-129-19insACCGTCCC
XM_006712021.2:c.-210-20_-210-19insACCGTCCC XP_006712084.1:n.-210-20_-210-19insACCGTCCC
XM_005264326.4:c.-5-20_-5-19insACCGTCCC XP_005264383.1:n.-5-20_-5-19insACCGTCCC
XM_006712021.3:c.-210-20_-210-19insACCGTCCC XP_006712084.1:n.-210-20_-210-19insACCGTCCC
XM_017004150.1:c.-3257-20_-3257-19insACCGTCCC XP_016859639.1:n.-3257-20_-3257-19insACCGTCCC
XM_024452913.1:c.-210-20_-210-19insACCGTCCC XP_024308681.1:n.-210-20_-210-19insACCGTCCC
NM_002437.5:c.-5-20_-5-19insACCGTCCC MANE Select NP_002428.1:n.-5-20_-5-19insACCGTCCC