Canonical Allele Identifier: CA1240217327

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313000G= , CM000664.2:g.27313000G=	GRCh38
NC_000002.11:g.27535867G= , CM000664.1:g.27535867G=	GRCh37
NC_000002.10:g.27389371G=	NCBI36
NG_008075.1:g.14565C=
NG_033055.1:g.264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.180C= MANE Select	ENSP00000369383.1:p.Gly60=
ENST00000233545.6:c.180C=	ENSP00000233545.2:p.Gly60=
ENST00000357186.10:c.19-228C=	ENSP00000349713.6:n.19-228C=
ENST00000380044.5:c.180C=	ENSP00000369383.1:p.Gly60=
ENST00000402310.5:c.180C=	ENSP00000383955.1:p.Gly60=
ENST00000402722.5:c.145C=	ENSP00000386000.1:p.Leu49=
ENST00000403262.6:c.180C=	ENSP00000385671.1:p.Gly60=
ENST00000405076.5:c.180C=	ENSP00000385175.1:p.Gly60=
ENST00000405983.5:c.225C=	ENSP00000384586.1:p.Gly75=
ENST00000415514.5:c.228-228C=	ENSP00000388043.1:n.228-228C=
ENST00000426513.6:c.145C=	ENSP00000403824.2:p.Leu49=
ENST00000428910.5:c.102C=	ENSP00000405235.1:p.Gly34=
ENST00000430991.5:c.110C=
ENST00000616446.1:n.157C=
ENST00000616707.1:n.388C=
ENST00000617583.4:n.206C=
ENST00000621183.4:n.236C=
ENST00000621470.4:n.196C=
ENST00000622003.4:n.353C=
NM_002437.4:c.180C=	NP_002428.1:p.Gly60=
XM_005264326.2:c.180C=	XP_005264383.1:p.Gly60=
XM_005264327.2:c.21C=	XP_005264384.1:p.Gly7=
XM_006712021.2:c.132C=	XP_006712084.1:p.Gly44=
XM_005264326.4:c.180C=	XP_005264383.1:p.Gly60=
XM_006712021.3:c.132C=	XP_006712084.1:p.Gly44=
XM_017004150.1:c.162C=	XP_016859639.1:p.Gly54=
XM_017004151.1:c.132C=	XP_016859640.1:p.Gly44=
XM_017004152.1:c.21C=	XP_016859641.1:p.Gly7=
XM_024452913.1:c.132C=	XP_024308681.1:p.Gly44=
NM_002437.5:c.180C= MANE Select	NP_002428.1:p.Gly60=