Canonical Allele Identifier: CA1240221776

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323066T= , CM000664.2:g.27323066T=	GRCh38
NC_000002.11:g.27545933T= , CM000664.1:g.27545933T=	GRCh37
NC_000002.10:g.27399437T=	NCBI36
NG_008075.1:g.4499A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.-20A= MANE Select	ENSP00000369383.1:n.-20A=
ENST00000357186.10:c.18+1367A=	ENSP00000349713.6:n.18+1367A=
ENST00000380044.5:c.-20A=	ENSP00000369383.1:n.-20A=
ENST00000399052.8:c.-20A=	ENSP00000382006.4:n.-20A=
ENST00000402722.5:c.-20A=	ENSP00000386000.1:n.-20A=
ENST00000403262.6:c.-20A=	ENSP00000385671.1:n.-20A=
ENST00000405076.5:c.-20A=	ENSP00000385175.1:n.-20A=
ENST00000426513.6:c.-20A=	ENSP00000403824.2:n.-20A=
ENST00000428910.5:c.-222A=	ENSP00000405235.1:n.-222A=
ENST00000486898.1:n.32A=
ENST00000494436.1:n.12A=
ENST00000617583.4:n.7A=
ENST00000621183.4:n.37A=
ENST00000621470.4:n.32A=
NM_002437.4:c.-20A=	NP_002428.1:n.-20A=
XM_005264327.2:c.-144A=	XP_005264384.1:n.-144A=
XM_006712021.2:c.-225A=	XP_006712084.1:n.-225A=
XM_005264326.4:c.-82A=	XP_005264383.1:n.-82A=
XM_006712021.3:c.-225A=	XP_006712084.1:n.-225A=
XM_017004150.1:c.-3272A=	XP_016859639.1:n.-3272A=
NM_002437.5:c.-20A= MANE Select	NP_002428.1:n.-20A=