Canonical Allele Identifier: CA1240221775

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323065C= , CM000664.2:g.27323065C=	GRCh38
NC_000002.11:g.27545932C= , CM000664.1:g.27545932C=	GRCh37
NC_000002.10:g.27399436C=	NCBI36
NG_008075.1:g.4500G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.-19G= MANE Select	ENSP00000369383.1:n.-19G=
ENST00000357186.10:c.18+1368G=	ENSP00000349713.6:n.18+1368G=
ENST00000380044.5:c.-19G=	ENSP00000369383.1:n.-19G=
ENST00000399052.8:c.-19G=	ENSP00000382006.4:n.-19G=
ENST00000402722.5:c.-19G=	ENSP00000386000.1:n.-19G=
ENST00000403262.6:c.-19G=	ENSP00000385671.1:n.-19G=
ENST00000405076.5:c.-19G=	ENSP00000385175.1:n.-19G=
ENST00000426513.6:c.-19G=	ENSP00000403824.2:n.-19G=
ENST00000428910.5:c.-221G=	ENSP00000405235.1:n.-221G=
ENST00000486898.1:n.33G=
ENST00000494436.1:n.13G=
ENST00000617583.4:n.8G=
ENST00000621183.4:n.38G=
ENST00000621470.4:n.33G=
NM_002437.4:c.-19G=	NP_002428.1:n.-19G=
XM_005264327.2:c.-143G=	XP_005264384.1:n.-143G=
XM_006712021.2:c.-224G=	XP_006712084.1:n.-224G=
XM_005264326.4:c.-81G=	XP_005264383.1:n.-81G=
XM_006712021.3:c.-224G=	XP_006712084.1:n.-224G=
XM_017004150.1:c.-3271G=	XP_016859639.1:n.-3271G=
NM_002437.5:c.-19G= MANE Select	NP_002428.1:n.-19G=