Canonical Allele Identifier: CA2658328533

Gene: MPV17

Linked Data

• gnomAD v4: 2-27323064-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323064C>A , CM000664.2:g.27323064C>A	GRCh38
NC_000002.11:g.27545931C>A , CM000664.1:g.27545931C>A	GRCh37
NC_000002.10:g.27399435C>A	NCBI36
NG_008075.1:g.4501G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-18G>T MANE Select	ENSP00000369383.1:n.-18G>T
ENST00000357186.10:c.18+1369G>T	ENSP00000349713.6:n.18+1369G>T
ENST00000380044.5:c.-18G>T	ENSP00000369383.1:n.-18G>T
ENST00000399052.8:c.-18G>T	ENSP00000382006.4:n.-18G>T
ENST00000402722.5:c.-18G>T	ENSP00000386000.1:n.-18G>T
ENST00000403262.6:c.-18G>T	ENSP00000385671.1:n.-18G>T
ENST00000405076.5:c.-18G>T	ENSP00000385175.1:n.-18G>T
ENST00000426513.6:c.-18G>T	ENSP00000403824.2:n.-18G>T
ENST00000428910.5:c.-220G>T	ENSP00000405235.1:n.-220G>T
ENST00000486898.1:n.34G>T
ENST00000494436.1:n.14G>T
ENST00000617583.4:n.9G>T
ENST00000621183.4:n.39G>T
ENST00000621470.4:n.34G>T
NM_002437.4:c.-18G>T	NP_002428.1:n.-18G>T
XM_005264327.2:c.-142G>T	XP_005264384.1:n.-142G>T
XM_006712021.2:c.-223G>T	XP_006712084.1:n.-223G>T
XM_005264326.4:c.-80G>T	XP_005264383.1:n.-80G>T
XM_006712021.3:c.-223G>T	XP_006712084.1:n.-223G>T
XM_017004150.1:c.-3270G>T	XP_016859639.1:n.-3270G>T
NM_002437.5:c.-18G>T MANE Select	NP_002428.1:n.-18G>T