Canonical Allele Identifier: CA1240215957

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27310137C= , CM000664.2:g.27310137C=	GRCh38
NC_000002.11:g.27533005C= , CM000664.1:g.27533005C=	GRCh37
NC_000002.10:g.27386509C=	NCBI36
NG_008075.1:g.17427G=
NG_033055.1:g.3126G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.462-156G= MANE Select	ENSP00000369383.1:n.462-156G=
ENST00000233545.6:c.462-156G=	ENSP00000233545.2:n.462-156G=
ENST00000357186.10:c.294-156G=	ENSP00000349713.6:n.294-156G=
ENST00000380044.5:c.462-156G=	ENSP00000369383.1:n.462-156G=
ENST00000402310.5:c.409-156G=	ENSP00000383955.1:n.409-156G=
ENST00000402722.5:c.*41-156G=	ENSP00000386000.1:n.*41-156G=
ENST00000405076.5:c.273-156G=	ENSP00000385175.1:n.273-156G=
ENST00000405983.5:c.507-156G=	ENSP00000384586.1:n.507-156G=
ENST00000415514.5:c.*263-156G=	ENSP00000388043.1:n.*263-156G=
ENST00000426513.6:c.*127-156G=	ENSP00000403824.2:n.*127-156G=
ENST00000430991.5:c.296-156G=
ENST00000620797.4:n.135-156G=
ENST00000621183.4:n.765-156G=
NM_002437.4:c.462-156G=	NP_002428.1:n.462-156G=
XM_005264326.2:c.462-156G=	XP_005264383.1:n.462-156G=
XM_005264327.2:c.303-156G=	XP_005264384.1:n.303-156G=
XM_006712021.2:c.414-156G=	XP_006712084.1:n.414-156G=
XM_005264326.4:c.462-156G=	XP_005264383.1:n.462-156G=
XM_006712021.3:c.414-156G=	XP_006712084.1:n.414-156G=
XM_017004150.1:c.444-156G=	XP_016859639.1:n.444-156G=
XM_017004151.1:c.414-156G=	XP_016859640.1:n.414-156G=
XM_017004152.1:c.303-156G=	XP_016859641.1:n.303-156G=
XM_024452913.1:c.414-156G=	XP_024308681.1:n.414-156G=
NM_002437.5:c.462-156G= MANE Select	NP_002428.1:n.462-156G=