Canonical Allele Identifier: CA1240215698

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309577G= , CM000664.2:g.27309577G=	GRCh38
NC_000002.11:g.27532445G= , CM000664.1:g.27532445G=	GRCh37
NC_000002.10:g.27385949G=	NCBI36
NG_008075.1:g.17987C=
NG_033055.1:g.3686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.*335C= MANE Select	ENSP00000369383.1:n.*335C=
ENST00000233545.6:c.*335C=	ENSP00000233545.2:n.*335C=
ENST00000357186.10:c.*335C=	ENSP00000349713.6:n.*335C=
ENST00000380044.5:c.*335C=	ENSP00000369383.1:n.*335C=
ENST00000402310.5:c.*300C=	ENSP00000383955.1:n.*300C=
ENST00000402722.5:c.*445C=	ENSP00000386000.1:n.*445C=
ENST00000426513.6:c.*531C=	ENSP00000403824.2:n.*531C=
ENST00000620797.4:n.539C=
NM_002437.4:c.*335C=	NP_002428.1:n.*335C=
XM_005264326.2:c.*335C=	XP_005264383.1:n.*335C=
XM_005264327.2:c.*335C=	XP_005264384.1:n.*335C=
XM_006712021.2:c.*335C=	XP_006712084.1:n.*335C=
XM_005264326.4:c.*335C=	XP_005264383.1:n.*335C=
XM_006712021.3:c.*335C=	XP_006712084.1:n.*335C=
XM_017004150.1:c.*335C=	XP_016859639.1:n.*335C=
XM_017004151.1:c.*335C=	XP_016859640.1:n.*335C=
XM_017004152.1:c.*335C=	XP_016859641.1:n.*335C=
XM_024452913.1:c.*335C=	XP_024308681.1:n.*335C=
NM_002437.5:c.*335C= MANE Select	NP_002428.1:n.*335C=