Canonical Allele Identifier: CA1240217104

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312514T= , CM000664.2:g.27312514T=	GRCh38
NC_000002.11:g.27535381T= , CM000664.1:g.27535381T=	GRCh37
NC_000002.10:g.27388885T=	NCBI36
NG_008075.1:g.15051A=
NG_033055.1:g.750A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.355A= MANE Select	ENSP00000369383.1:p.Asn119=
ENST00000233545.6:c.355A=	ENSP00000233545.2:p.Asn119=
ENST00000357186.10:c.187A=	ENSP00000349713.6:p.Asn63=
ENST00000380044.5:c.355A=	ENSP00000369383.1:p.Asn119=
ENST00000402310.5:c.355A=	ENSP00000383955.1:p.Asn119=
ENST00000402722.5:c.*20A=	ENSP00000386000.1:n.*20A=
ENST00000403262.6:c.355A=	ENSP00000385671.1:p.Asn119=
ENST00000405076.5:c.187-268A=	ENSP00000385175.1:n.187-268A=
ENST00000405983.5:c.400A=	ENSP00000384586.1:p.Asn134=
ENST00000415514.5:c.*156A=	ENSP00000388043.1:n.*156A=
ENST00000426513.6:c.*20A=	ENSP00000403824.2:n.*20A=
ENST00000428910.5:c.277A=	ENSP00000405235.1:p.Asn93=
ENST00000430991.5:c.209+166A=
ENST00000475085.1:n.383A=
ENST00000616446.1:n.332A=
ENST00000616707.1:n.874A=
ENST00000617583.4:n.381A=
ENST00000621183.4:n.411A=
ENST00000621470.4:n.371A=
ENST00000622003.4:n.528A=
NM_002437.4:c.355A=	NP_002428.1:p.Asn119=
XM_005264326.2:c.355A=	XP_005264383.1:p.Asn119=
XM_005264327.2:c.196A=	XP_005264384.1:p.Asn66=
XM_006712021.2:c.307A=	XP_006712084.1:p.Asn103=
XM_005264326.4:c.355A=	XP_005264383.1:p.Asn119=
XM_006712021.3:c.307A=	XP_006712084.1:p.Asn103=
XM_017004150.1:c.337A=	XP_016859639.1:p.Asn113=
XM_017004151.1:c.307A=	XP_016859640.1:p.Asn103=
XM_017004152.1:c.196A=	XP_016859641.1:p.Asn66=
XM_024452913.1:c.307A=	XP_024308681.1:p.Asn103=
NM_002437.5:c.355A= MANE Select	NP_002428.1:p.Asn119=