Canonical Allele Identifier: CA1240221474

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27322456A= , CM000664.2:g.27322456A=	GRCh38
NC_000002.11:g.27545323A= , CM000664.1:g.27545323A=	GRCh37
NC_000002.10:g.27398827A=	NCBI36
NG_008075.1:g.5109T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.62T= MANE Select	ENSP00000369383.1:p.Leu21=
ENST00000233545.6:c.62T=	ENSP00000233545.2:p.Leu21=
ENST00000357186.10:c.18+1977T=	ENSP00000349713.6:n.18+1977T=
ENST00000380044.5:c.62T=	ENSP00000369383.1:p.Leu21=
ENST00000399052.8:c.62T=	ENSP00000382006.4:p.Leu21=
ENST00000402310.5:c.62T=	ENSP00000383955.1:p.Leu21=
ENST00000402722.5:c.62T=	ENSP00000386000.1:p.Leu21=
ENST00000403262.6:c.62T=	ENSP00000385671.1:p.Leu21=
ENST00000405076.5:c.62T=	ENSP00000385175.1:p.Leu21=
ENST00000405983.5:c.62T=	ENSP00000384586.1:p.Leu21=
ENST00000415514.5:c.62T=	ENSP00000388043.1:p.Leu21=
ENST00000426513.6:c.62T=	ENSP00000403824.2:p.Leu21=
ENST00000428910.5:c.-141T=	ENSP00000405235.1:n.-141T=
ENST00000486898.1:n.113T=
ENST00000494436.1:n.93T=
ENST00000617583.4:n.88T=
ENST00000621183.4:n.118T=
ENST00000621470.4:n.113T=
ENST00000622003.4:n.78T=
NM_002437.4:c.62T=	NP_002428.1:p.Leu21=
XM_005264326.2:c.62T=	XP_005264383.1:p.Leu21=
XM_005264327.2:c.-63T=	XP_005264384.1:n.-63T=
XM_006712021.2:c.-144T=	XP_006712084.1:n.-144T=
XM_005264326.4:c.62T=	XP_005264383.1:p.Leu21=
XM_006712021.3:c.-144T=	XP_006712084.1:n.-144T=
XM_017004150.1:c.-3191T=	XP_016859639.1:n.-3191T=
XM_017004151.1:c.-83T=	XP_016859640.1:n.-83T=
XM_017004152.1:c.-220T=	XP_016859641.1:n.-220T=
XM_024452913.1:c.-144T=	XP_024308681.1:n.-144T=
NM_002437.5:c.62T= MANE Select	NP_002428.1:p.Leu21=