Canonical Allele Identifier: CA2658328531
Gene: MPV17 HGNC NCBI

Linked Data

gnomAD v4: 2-27323062-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323062A>T , CM000664.2:g.27323062A>T GRCh38
NC_000002.11:g.27545929A>T , CM000664.1:g.27545929A>T GRCh37
NC_000002.10:g.27399433A>T NCBI36
NG_008075.1:g.4503T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.-16T>A MANE Select ENSP00000369383.1:n.-16T>A
ENST00000357186.10:c.18+1371T>A ENSP00000349713.6:n.18+1371T>A
ENST00000380044.5:c.-16T>A ENSP00000369383.1:n.-16T>A
ENST00000399052.8:c.-16T>A ENSP00000382006.4:n.-16T>A
ENST00000402722.5:c.-16T>A ENSP00000386000.1:n.-16T>A
ENST00000403262.6:c.-16T>A ENSP00000385671.1:n.-16T>A
ENST00000405076.5:c.-16T>A ENSP00000385175.1:n.-16T>A
ENST00000405983.5:c.-16T>A ENSP00000384586.1:n.-16T>A
ENST00000415514.5:c.-16T>A ENSP00000388043.1:n.-16T>A
ENST00000426513.6:c.-16T>A ENSP00000403824.2:n.-16T>A
ENST00000428910.5:c.-218T>A ENSP00000405235.1:n.-218T>A
ENST00000486898.1:n.36T>A
ENST00000494436.1:n.16T>A
ENST00000617583.4:n.11T>A
ENST00000621183.4:n.41T>A
ENST00000621470.4:n.36T>A
ENST00000622003.4:n.1T>A
NM_002437.4:c.-16T>A NP_002428.1:n.-16T>A
XM_005264327.2:c.-140T>A XP_005264384.1:n.-140T>A
XM_006712021.2:c.-221T>A XP_006712084.1:n.-221T>A
XM_005264326.4:c.-78T>A XP_005264383.1:n.-78T>A
XM_006712021.3:c.-221T>A XP_006712084.1:n.-221T>A
XM_017004150.1:c.-3268T>A XP_016859639.1:n.-3268T>A
NM_002437.5:c.-16T>A MANE Select NP_002428.1:n.-16T>A