Canonical Allele Identifier: CA1240217187

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312692C= , CM000664.2:g.27312692C=	GRCh38
NC_000002.11:g.27535559C= , CM000664.1:g.27535559C=	GRCh37
NC_000002.10:g.27389063C=	NCBI36
NG_008075.1:g.14873G=
NG_033055.1:g.572G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.267G= MANE Select	ENSP00000369383.1:p.Met89=
ENST00000233545.6:c.267G=	ENSP00000233545.2:p.Met89=
ENST00000357186.10:c.99G=	ENSP00000349713.6:p.Met33=
ENST00000380044.5:c.267G=	ENSP00000369383.1:p.Met89=
ENST00000402310.5:c.267G=	ENSP00000383955.1:p.Met89=
ENST00000402722.5:c.232G=	ENSP00000386000.1:p.Val78=
ENST00000403262.6:c.267G=	ENSP00000385671.1:p.Met89=
ENST00000405076.5:c.186+302G=	ENSP00000385175.1:n.186+302G=
ENST00000405983.5:c.312G=	ENSP00000384586.1:p.Met104=
ENST00000415514.5:c.*68G=	ENSP00000388043.1:n.*68G=
ENST00000426513.6:c.232G=	ENSP00000403824.2:p.Val78=
ENST00000428910.5:c.189G=	ENSP00000405235.1:p.Met63=
ENST00000430991.5:c.197G=
ENST00000475085.1:n.295G=
ENST00000616446.1:n.244G=
ENST00000616707.1:n.696G=
ENST00000617583.4:n.293G=
ENST00000621183.4:n.323G=
ENST00000621470.4:n.283G=
ENST00000622003.4:n.440G=
NM_002437.4:c.267G=	NP_002428.1:p.Met89=
XM_005264326.2:c.267G=	XP_005264383.1:p.Met89=
XM_005264327.2:c.108G=	XP_005264384.1:p.Met36=
XM_006712021.2:c.219G=	XP_006712084.1:p.Met73=
XM_005264326.4:c.267G=	XP_005264383.1:p.Met89=
XM_006712021.3:c.219G=	XP_006712084.1:p.Met73=
XM_017004150.1:c.249G=	XP_016859639.1:p.Met83=
XM_017004151.1:c.219G=	XP_016859640.1:p.Met73=
XM_017004152.1:c.108G=	XP_016859641.1:p.Met36=
XM_024452913.1:c.219G=	XP_024308681.1:p.Met73=
NM_002437.5:c.267G= MANE Select	NP_002428.1:p.Met89=