Canonical Allele Identifier: CA1240221785

Gene: MPV17

Genomic Alleles

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

Transcript Alleles

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