Canonical Allele Identifier: CA2658328559

Gene: MPV17

Linked Data

• gnomAD v4: 2-27323087-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323087G>T , CM000664.2:g.27323087G>T	GRCh38
NC_000002.11:g.27545954G>T , CM000664.1:g.27545954G>T	GRCh37
NC_000002.10:g.27399458G>T	NCBI36
NG_008075.1:g.4478C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-41C>A MANE Select	ENSP00000369383.1:n.-41C>A
ENST00000357186.10:c.18+1346C>A	ENSP00000349713.6:n.18+1346C>A
ENST00000380044.5:c.-41C>A	ENSP00000369383.1:n.-41C>A
ENST00000399052.8:c.-41C>A	ENSP00000382006.4:n.-41C>A
ENST00000405076.5:c.-41C>A	ENSP00000385175.1:n.-41C>A
ENST00000486898.1:n.11C>A
ENST00000621183.4:n.16C>A
ENST00000621470.4:n.11C>A
NM_002437.4:c.-41C>A	NP_002428.1:n.-41C>A
XM_005264327.2:c.-165C>A	XP_005264384.1:n.-165C>A
XM_006712021.2:c.-246C>A	XP_006712084.1:n.-246C>A
XM_006712021.3:c.-246C>A	XP_006712084.1:n.-246C>A
XM_017004150.1:c.-3293C>A	XP_016859639.1:n.-3293C>A
NM_002437.5:c.-41C>A MANE Select	NP_002428.1:n.-41C>A