Canonical Allele Identifier: CA1028674833
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1679911620
gnomAD v3: 2-27322959-G-A
gnomAD v4: 2-27322959-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27322959G>A , CM000664.2:g.27322959G>A GRCh38
NC_000002.11:g.27545826G>A , CM000664.1:g.27545826G>A GRCh37
NC_000002.10:g.27399330G>A NCBI36
NG_008075.1:g.4606C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.-6+93C>T MANE Select ENSP00000369383.1:n.-6+93C>T
ENST00000357186.10:c.18+1474C>T ENSP00000349713.6:n.18+1474C>T
ENST00000380044.5:c.-6+93C>T ENSP00000369383.1:n.-6+93C>T
ENST00000399052.8:c.-6+93C>T ENSP00000382006.4:n.-6+93C>T
ENST00000402310.5:c.-6+93C>T ENSP00000383955.1:n.-6+93C>T
ENST00000402722.5:c.-6+93C>T ENSP00000386000.1:n.-6+93C>T
ENST00000403262.6:c.-6+93C>T ENSP00000385671.1:n.-6+93C>T
ENST00000405076.5:c.-6+93C>T ENSP00000385175.1:n.-6+93C>T
ENST00000405983.5:c.-6+93C>T ENSP00000384586.1:n.-6+93C>T
ENST00000415514.5:c.-6+93C>T ENSP00000388043.1:n.-6+93C>T
ENST00000426513.6:c.-6+93C>T ENSP00000403824.2:n.-6+93C>T
ENST00000428910.5:c.-208+93C>T ENSP00000405235.1:n.-208+93C>T
ENST00000486898.1:n.46+93C>T
ENST00000494436.1:n.26+93C>T
ENST00000617583.4:n.21+93C>T
ENST00000621183.4:n.51+93C>T
ENST00000621470.4:n.46+93C>T
ENST00000622003.4:n.11+93C>T
NM_002437.4:c.-6+93C>T NP_002428.1:n.-6+93C>T
XM_005264326.2:c.-6+31C>T XP_005264383.1:n.-6+31C>T
XM_005264327.2:c.-130+93C>T XP_005264384.1:n.-130+93C>T
XM_006712021.2:c.-211+93C>T XP_006712084.1:n.-211+93C>T
XM_005264326.4:c.-6+31C>T XP_005264383.1:n.-6+31C>T
XM_006712021.3:c.-211+93C>T XP_006712084.1:n.-211+93C>T
XM_017004150.1:c.-3258+93C>T XP_016859639.1:n.-3258+93C>T
XM_024452913.1:c.-211+31C>T XP_024308681.1:n.-211+31C>T
NM_002437.5:c.-6+93C>T MANE Select NP_002428.1:n.-6+93C>T