Canonical Allele Identifier: CA1240216820

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27311926T= , CM000664.2:g.27311926T=	GRCh38
NC_000002.11:g.27534794T= , CM000664.1:g.27534794T=	GRCh37
NC_000002.10:g.27388298T=	NCBI36
NG_008075.1:g.15638A=
NG_033055.1:g.1337A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.434A= MANE Select	ENSP00000369383.1:p.Asn145=
ENST00000233545.6:c.434A=	ENSP00000233545.2:p.Asn145=
ENST00000357186.10:c.266A=	ENSP00000349713.6:p.Asn89=
ENST00000380044.5:c.434A=	ENSP00000369383.1:p.Asn145=
ENST00000402310.5:c.408+288A=	ENSP00000383955.1:n.408+288A=
ENST00000402722.5:c.*40+568A=	ENSP00000386000.1:n.*40+568A=
ENST00000403262.6:c.434A=	ENSP00000385671.1:p.Asn145=
ENST00000405076.5:c.245A=	ENSP00000385175.1:p.Asn82=
ENST00000405983.5:c.479A=	ENSP00000384586.1:p.Asn160=
ENST00000415514.5:c.*235A=	ENSP00000388043.1:n.*235A=
ENST00000426513.6:c.*99A=	ENSP00000403824.2:n.*99A=
ENST00000430991.5:c.268A=
ENST00000616707.1:n.1462A=
ENST00000620797.4:n.107A=
ENST00000621183.4:n.737A=
NM_002437.4:c.434A=	NP_002428.1:p.Asn145=
XM_005264326.2:c.434A=	XP_005264383.1:p.Asn145=
XM_005264327.2:c.275A=	XP_005264384.1:p.Asn92=
XM_006712021.2:c.386A=	XP_006712084.1:p.Asn129=
XM_005264326.4:c.434A=	XP_005264383.1:p.Asn145=
XM_006712021.3:c.386A=	XP_006712084.1:p.Asn129=
XM_017004150.1:c.416A=	XP_016859639.1:p.Asn139=
XM_017004151.1:c.386A=	XP_016859640.1:p.Asn129=
XM_017004152.1:c.275A=	XP_016859641.1:p.Asn92=
XM_024452913.1:c.386A=	XP_024308681.1:p.Asn129=
NM_002437.5:c.434A= MANE Select	NP_002428.1:p.Asn145=