Canonical Allele Identifier: CA1240221786

Gene: MPV17

Linked Data

• dbSNP Id: rs1572556002

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323077T>C , CM000664.2:g.27323077T>C	GRCh38
NC_000002.11:g.27545944T>C , CM000664.1:g.27545944T>C	GRCh37
NC_000002.10:g.27399448T>C	NCBI36
NG_008075.1:g.4488A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-31A>G MANE Select	ENSP00000369383.1:n.-31A>G
ENST00000357186.10:c.18+1356A>G	ENSP00000349713.6:n.18+1356A>G
ENST00000380044.5:c.-31A>G	ENSP00000369383.1:n.-31A>G
ENST00000399052.8:c.-31A>G	ENSP00000382006.4:n.-31A>G
ENST00000402722.5:c.-31A>G	ENSP00000386000.1:n.-31A>G
ENST00000405076.5:c.-31A>G	ENSP00000385175.1:n.-31A>G
ENST00000426513.6:c.-31A>G	ENSP00000403824.2:n.-31A>G
ENST00000486898.1:n.21A>G
ENST00000494436.1:n.1A>G
ENST00000621183.4:n.26A>G
ENST00000621470.4:n.21A>G
NM_002437.4:c.-31A>G	NP_002428.1:n.-31A>G
XM_005264327.2:c.-155A>G	XP_005264384.1:n.-155A>G
XM_006712021.2:c.-236A>G	XP_006712084.1:n.-236A>G
XM_006712021.3:c.-236A>G	XP_006712084.1:n.-236A>G
XM_017004150.1:c.-3283A>G	XP_016859639.1:n.-3283A>G
NM_002437.5:c.-31A>G MANE Select	NP_002428.1:n.-31A>G