Canonical Allele Identifier: CA346205263

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532759A>G (hg19) ; chr2:g.27309891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309891A>G , CM000664.2:g.27309891A>G	GRCh38
NC_000002.11:g.27532759A>G , CM000664.1:g.27532759A>G	GRCh37
NC_000002.10:g.27386263A>G	NCBI36
NG_008075.1:g.17673T>C
NG_033055.1:g.3372T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.*21T>C MANE Select	ENSP00000369383.1:n.*21T>C
ENST00000233545.6:c.*21T>C	ENSP00000233545.2:n.*21T>C
ENST00000357186.10:c.*21T>C	ENSP00000349713.6:n.*21T>C
ENST00000380044.5:c.*21T>C	ENSP00000369383.1:n.*21T>C
ENST00000402310.5:c.499T>C	ENSP00000383955.1:p.Ser167Pro
ENST00000402722.5:c.*131T>C	ENSP00000386000.1:n.*131T>C
ENST00000405076.5:c.*21T>C	ENSP00000385175.1:n.*21T>C
ENST00000405983.5:c.*21T>C	ENSP00000384586.1:n.*21T>C
ENST00000426513.6:c.*217T>C	ENSP00000403824.2:n.*217T>C
ENST00000430991.5:c.386T>C
ENST00000620797.4:n.225T>C
ENST00000621183.4:n.855T>C
NM_002437.4:c.*21T>C	NP_002428.1:n.*21T>C
XM_005264326.2:c.*21T>C	XP_005264383.1:n.*21T>C
XM_005264327.2:c.*21T>C	XP_005264384.1:n.*21T>C
XM_006712021.2:c.*21T>C	XP_006712084.1:n.*21T>C
XM_005264326.4:c.*21T>C	XP_005264383.1:n.*21T>C
XM_006712021.3:c.*21T>C	XP_006712084.1:n.*21T>C
XM_017004150.1:c.*21T>C	XP_016859639.1:n.*21T>C
XM_017004151.1:c.*21T>C	XP_016859640.1:n.*21T>C
XM_017004152.1:c.*21T>C	XP_016859641.1:n.*21T>C
XM_024452913.1:c.*21T>C	XP_024308681.1:n.*21T>C
NM_002437.5:c.*21T>C MANE Select	NP_002428.1:n.*21T>C