Canonical Allele Identifier: CA1240221771

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323058G= , CM000664.2:g.27323058G=	GRCh38
NC_000002.11:g.27545925G= , CM000664.1:g.27545925G=	GRCh37
NC_000002.10:g.27399429G=	NCBI36
NG_008075.1:g.4507C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.-12C= MANE Select	ENSP00000369383.1:n.-12C=
ENST00000357186.10:c.18+1375C=	ENSP00000349713.6:n.18+1375C=
ENST00000380044.5:c.-12C=	ENSP00000369383.1:n.-12C=
ENST00000399052.8:c.-12C=	ENSP00000382006.4:n.-12C=
ENST00000402722.5:c.-12C=	ENSP00000386000.1:n.-12C=
ENST00000403262.6:c.-12C=	ENSP00000385671.1:n.-12C=
ENST00000405076.5:c.-12C=	ENSP00000385175.1:n.-12C=
ENST00000405983.5:c.-12C=	ENSP00000384586.1:n.-12C=
ENST00000415514.5:c.-12C=	ENSP00000388043.1:n.-12C=
ENST00000426513.6:c.-12C=	ENSP00000403824.2:n.-12C=
ENST00000428910.5:c.-214C=	ENSP00000405235.1:n.-214C=
ENST00000486898.1:n.40C=
ENST00000494436.1:n.20C=
ENST00000617583.4:n.15C=
ENST00000621183.4:n.45C=
ENST00000621470.4:n.40C=
ENST00000622003.4:n.5C=
NM_002437.4:c.-12C=	NP_002428.1:n.-12C=
XM_005264327.2:c.-136C=	XP_005264384.1:n.-136C=
XM_006712021.2:c.-217C=	XP_006712084.1:n.-217C=
XM_005264326.4:c.-74C=	XP_005264383.1:n.-74C=
XM_006712021.3:c.-217C=	XP_006712084.1:n.-217C=
XM_017004150.1:c.-3264C=	XP_016859639.1:n.-3264C=
XM_024452913.1:c.-279C=	XP_024308681.1:n.-279C=
NM_002437.5:c.-12C= MANE Select	NP_002428.1:n.-12C=