Canonical Allele Identifier: CA2658328560
Gene: MPV17 HGNC NCBI

Linked Data

gnomAD v4: 2-27323088-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323088C>A , CM000664.2:g.27323088C>A GRCh38
NC_000002.11:g.27545955C>A , CM000664.1:g.27545955C>A GRCh37
NC_000002.10:g.27399459C>A NCBI36
NG_008075.1:g.4477G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.-42G>T MANE Select ENSP00000369383.1:n.-42G>T
ENST00000357186.10:c.18+1345G>T ENSP00000349713.6:n.18+1345G>T
ENST00000380044.5:c.-42G>T ENSP00000369383.1:n.-42G>T
ENST00000399052.8:c.-42G>T ENSP00000382006.4:n.-42G>T
ENST00000405076.5:c.-42G>T ENSP00000385175.1:n.-42G>T
ENST00000486898.1:n.10G>T
ENST00000621183.4:n.15G>T
ENST00000621470.4:n.10G>T
NM_002437.4:c.-42G>T NP_002428.1:n.-42G>T
XM_005264327.2:c.-166G>T XP_005264384.1:n.-166G>T
XM_006712021.2:c.-247G>T XP_006712084.1:n.-247G>T
XM_006712021.3:c.-247G>T XP_006712084.1:n.-247G>T
XM_017004150.1:c.-3294G>T XP_016859639.1:n.-3294G>T
NM_002437.5:c.-42G>T MANE Select NP_002428.1:n.-42G>T