Canonical Allele Identifier: CA2658328536

Gene: MPV17

Linked Data

• gnomAD v4: 2-27323066-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323069del , CM000664.2:g.27323069del	GRCh38
NC_000002.11:g.27545936del , CM000664.1:g.27545936del	GRCh37
NC_000002.10:g.27399440del	NCBI36
NG_008075.1:g.4498del

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.-21del MANE Select	ENSP00000369383.1:n.-21del
ENST00000357186.10:c.18+1366del	ENSP00000349713.6:n.18+1366del
ENST00000380044.5:c.-21del	ENSP00000369383.1:n.-21del
ENST00000399052.8:c.-21del	ENSP00000382006.4:n.-21del
ENST00000402722.5:c.-21del	ENSP00000386000.1:n.-21del
ENST00000405076.5:c.-21del	ENSP00000385175.1:n.-21del
ENST00000426513.6:c.-21del	ENSP00000403824.2:n.-21del
ENST00000428910.5:c.-223del	ENSP00000405235.1:n.-223del
ENST00000486898.1:n.31del
ENST00000494436.1:n.11del
ENST00000617583.4:n.6del
ENST00000621183.4:n.36del
ENST00000621470.4:n.31del
NM_002437.4:c.-21del	NP_002428.1:n.-21del
XM_005264327.2:c.-145del	XP_005264384.1:n.-145del
XM_006712021.2:c.-226del	XP_006712084.1:n.-226del
XM_006712021.3:c.-226del	XP_006712084.1:n.-226del
XM_017004150.1:c.-3273del	XP_016859639.1:n.-3273del
NM_002437.5:c.-21del MANE Select	NP_002428.1:n.-21del