Canonical Allele Identifier: CA346205274

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532765T>G (hg19) ; chr2:g.27309897T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309897T>G , CM000664.2:g.27309897T>G	GRCh38
NC_000002.11:g.27532765T>G , CM000664.1:g.27532765T>G	GRCh37
NC_000002.10:g.27386269T>G	NCBI36
NG_008075.1:g.17667A>C
NG_033055.1:g.3366A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.*15A>C MANE Select	ENSP00000369383.1:n.*15A>C
ENST00000233545.6:c.*15A>C	ENSP00000233545.2:n.*15A>C
ENST00000357186.10:c.*15A>C	ENSP00000349713.6:n.*15A>C
ENST00000380044.5:c.*15A>C	ENSP00000369383.1:n.*15A>C
ENST00000402310.5:c.493A>C	ENSP00000383955.1:p.Ile165Leu
ENST00000402722.5:c.*125A>C	ENSP00000386000.1:n.*125A>C
ENST00000405076.5:c.*15A>C	ENSP00000385175.1:n.*15A>C
ENST00000405983.5:c.*15A>C	ENSP00000384586.1:n.*15A>C
ENST00000426513.6:c.*211A>C	ENSP00000403824.2:n.*211A>C
ENST00000430991.5:c.380A>C
ENST00000620797.4:n.219A>C
ENST00000621183.4:n.849A>C
NM_002437.4:c.*15A>C	NP_002428.1:n.*15A>C
XM_005264326.2:c.*15A>C	XP_005264383.1:n.*15A>C
XM_005264327.2:c.*15A>C	XP_005264384.1:n.*15A>C
XM_006712021.2:c.*15A>C	XP_006712084.1:n.*15A>C
XM_005264326.4:c.*15A>C	XP_005264383.1:n.*15A>C
XM_006712021.3:c.*15A>C	XP_006712084.1:n.*15A>C
XM_017004150.1:c.*15A>C	XP_016859639.1:n.*15A>C
XM_017004151.1:c.*15A>C	XP_016859640.1:n.*15A>C
XM_017004152.1:c.*15A>C	XP_016859641.1:n.*15A>C
XM_024452913.1:c.*15A>C	XP_024308681.1:n.*15A>C
NM_002437.5:c.*15A>C MANE Select	NP_002428.1:n.*15A>C