Canonical Allele Identifier: CA646578150

Gene: MPV17

Linked Data

• gnomAD v4: 2-27323089-C-A
• COSMIC: COSN9369119

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323089C>A , CM000664.2:g.27323089C>A	GRCh38
NC_000002.11:g.27545956C>A , CM000664.1:g.27545956C>A	GRCh37
NC_000002.10:g.27399460C>A	NCBI36
NG_008075.1:g.4476G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-43G>T MANE Select	ENSP00000369383.1:n.-43G>T
ENST00000357186.10:c.18+1344G>T	ENSP00000349713.6:n.18+1344G>T
ENST00000380044.5:c.-43G>T	ENSP00000369383.1:n.-43G>T
ENST00000399052.8:c.-43G>T	ENSP00000382006.4:n.-43G>T
ENST00000405076.5:c.-43G>T	ENSP00000385175.1:n.-43G>T
ENST00000486898.1:n.9G>T
ENST00000621183.4:n.14G>T
ENST00000621470.4:n.9G>T
NM_002437.4:c.-43G>T	NP_002428.1:n.-43G>T
XM_005264327.2:c.-167G>T	XP_005264384.1:n.-167G>T
XM_006712021.2:c.-248G>T	XP_006712084.1:n.-248G>T
XM_006712021.3:c.-248G>T	XP_006712084.1:n.-248G>T
XM_017004150.1:c.-3295G>T	XP_016859639.1:n.-3295G>T
NM_002437.5:c.-43G>T MANE Select	NP_002428.1:n.-43G>T