Canonical Allele Identifier: CA1240215872

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309966T= , CM000664.2:g.27309966T=	GRCh38
NC_000002.11:g.27532834T= , CM000664.1:g.27532834T=	GRCh37
NC_000002.10:g.27386338T=	NCBI36
NG_008075.1:g.17598A=
NG_033055.1:g.3297A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.477A= MANE Select	ENSP00000369383.1:p.Gln159=
ENST00000233545.6:c.477A=	ENSP00000233545.2:p.Gln159=
ENST00000357186.10:c.309A=	ENSP00000349713.6:p.Gln103=
ENST00000380044.5:c.477A=	ENSP00000369383.1:p.Gln159=
ENST00000402310.5:c.424A=	ENSP00000383955.1:p.Met142=
ENST00000402722.5:c.*56A=	ENSP00000386000.1:n.*56A=
ENST00000405076.5:c.288A=	ENSP00000385175.1:p.Gln96=
ENST00000405983.5:c.522A=	ENSP00000384586.1:p.Gln174=
ENST00000415514.5:c.*278A=	ENSP00000388043.1:n.*278A=
ENST00000426513.6:c.*142A=	ENSP00000403824.2:n.*142A=
ENST00000430991.5:c.311A=
ENST00000620797.4:n.150A=
ENST00000621183.4:n.780A=
NM_002437.4:c.477A=	NP_002428.1:p.Gln159=
XM_005264326.2:c.477A=	XP_005264383.1:p.Gln159=
XM_005264327.2:c.318A=	XP_005264384.1:p.Gln106=
XM_006712021.2:c.429A=	XP_006712084.1:p.Gln143=
XM_005264326.4:c.477A=	XP_005264383.1:p.Gln159=
XM_006712021.3:c.429A=	XP_006712084.1:p.Gln143=
XM_017004150.1:c.459A=	XP_016859639.1:p.Gln153=
XM_017004151.1:c.429A=	XP_016859640.1:p.Gln143=
XM_017004152.1:c.318A=	XP_016859641.1:p.Gln106=
XM_024452913.1:c.429A=	XP_024308681.1:p.Gln143=
NM_002437.5:c.477A= MANE Select	NP_002428.1:p.Gln159=