Canonical Allele Identifier: CA346209322

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535905T>G (hg19) ; chr2:g.27313038T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313038T>G , CM000664.2:g.27313038T>G	GRCh38
NC_000002.11:g.27535905T>G , CM000664.1:g.27535905T>G	GRCh37
NC_000002.10:g.27389409T>G	NCBI36
NG_008075.1:g.14527A>C
NG_033055.1:g.226A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.142A>C MANE Select	ENSP00000369383.1:p.Arg48=
ENST00000233545.6:c.142A>C	ENSP00000233545.2:p.Arg48=
ENST00000357186.10:c.19-266A>C	ENSP00000349713.6:n.19-266A>C
ENST00000380044.5:c.142A>C	ENSP00000369383.1:p.Arg48=
ENST00000402310.5:c.142A>C	ENSP00000383955.1:p.Arg48=
ENST00000402722.5:c.107A>C	ENSP00000386000.1:p.Glu36Ala
ENST00000403262.6:c.142A>C	ENSP00000385671.1:p.Arg48=
ENST00000405076.5:c.142A>C	ENSP00000385175.1:p.Arg48=
ENST00000405983.5:c.187A>C	ENSP00000384586.1:p.Arg63=
ENST00000415514.5:c.228-266A>C	ENSP00000388043.1:n.228-266A>C
ENST00000426513.6:c.107A>C	ENSP00000403824.2:p.Glu36Ala
ENST00000428910.5:c.64A>C	ENSP00000405235.1:p.Arg22=
ENST00000430991.5:c.72A>C
ENST00000616446.1:n.119A>C
ENST00000616707.1:n.350A>C
ENST00000617583.4:n.168A>C
ENST00000621183.4:n.198A>C
ENST00000621470.4:n.158A>C
ENST00000622003.4:n.315A>C
NM_002437.4:c.142A>C	NP_002428.1:p.Arg48=
XM_005264326.2:c.142A>C	XP_005264383.1:p.Arg48=
XM_005264327.2:c.-18A>C	XP_005264384.1:n.-18A>C
XM_006712021.2:c.94A>C	XP_006712084.1:p.Arg32=
XM_005264326.4:c.142A>C	XP_005264383.1:p.Arg48=
XM_006712021.3:c.94A>C	XP_006712084.1:p.Arg32=
XM_017004150.1:c.124A>C	XP_016859639.1:p.Arg42=
XM_017004151.1:c.94A>C	XP_016859640.1:p.Arg32=
XM_017004152.1:c.-18A>C	XP_016859641.1:n.-18A>C
XM_024452913.1:c.94A>C	XP_024308681.1:p.Arg32=
NM_002437.5:c.142A>C MANE Select	NP_002428.1:p.Arg48=