Canonical Allele Identifier: CA2658328563

Gene: MPV17

Linked Data

• dbSNP Id: rs2148226208
• gnomAD v4: 2-27323091-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323091A>G , CM000664.2:g.27323091A>G	GRCh38
NC_000002.11:g.27545958A>G , CM000664.1:g.27545958A>G	GRCh37
NC_000002.10:g.27399462A>G	NCBI36
NG_008075.1:g.4474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-45T>C MANE Select	ENSP00000369383.1:n.-45T>C
ENST00000357186.10:c.18+1342T>C	ENSP00000349713.6:n.18+1342T>C
ENST00000380044.5:c.-45T>C	ENSP00000369383.1:n.-45T>C
ENST00000399052.8:c.-45T>C	ENSP00000382006.4:n.-45T>C
ENST00000405076.5:c.-45T>C	ENSP00000385175.1:n.-45T>C
ENST00000486898.1:n.7T>C
ENST00000621183.4:n.12T>C
ENST00000621470.4:n.7T>C
NM_002437.4:c.-45T>C	NP_002428.1:n.-45T>C
XM_005264327.2:c.-169T>C	XP_005264384.1:n.-169T>C
XM_006712021.2:c.-250T>C	XP_006712084.1:n.-250T>C
XM_006712021.3:c.-250T>C	XP_006712084.1:n.-250T>C
XM_017004150.1:c.-3297T>C	XP_016859639.1:n.-3297T>C
NM_002437.5:c.-45T>C MANE Select	NP_002428.1:n.-45T>C