Canonical Allele Identifier: CA346209442

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535935C>G (hg19) ; chr2:g.27313068C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313068C>G , CM000664.2:g.27313068C>G	GRCh38
NC_000002.11:g.27535935C>G , CM000664.1:g.27535935C>G	GRCh37
NC_000002.10:g.27389439C>G	NCBI36
NG_008075.1:g.14497G>C
NG_033055.1:g.196G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.112G>C MANE Select	ENSP00000369383.1:p.Val38Leu
ENST00000233545.6:c.112G>C	ENSP00000233545.2:p.Val38Leu
ENST00000357186.10:c.19-296G>C	ENSP00000349713.6:n.19-296G>C
ENST00000380044.5:c.112G>C	ENSP00000369383.1:p.Val38Leu
ENST00000402310.5:c.112G>C	ENSP00000383955.1:p.Val38Leu
ENST00000402722.5:c.77G>C	ENSP00000386000.1:p.Gly26Ala
ENST00000403262.6:c.112G>C	ENSP00000385671.1:p.Val38Leu
ENST00000405076.5:c.112G>C	ENSP00000385175.1:p.Val38Leu
ENST00000405983.5:c.157G>C	ENSP00000384586.1:p.Val53Leu
ENST00000415514.5:c.228-296G>C	ENSP00000388043.1:n.228-296G>C
ENST00000426513.6:c.77G>C	ENSP00000403824.2:p.Gly26Ala
ENST00000428910.5:c.34G>C	ENSP00000405235.1:p.Val12Leu
ENST00000430991.5:c.42G>C
ENST00000616446.1:n.89G>C
ENST00000616707.1:n.320G>C
ENST00000617583.4:n.138G>C
ENST00000621183.4:n.168G>C
ENST00000621470.4:n.128G>C
ENST00000622003.4:n.285G>C
NM_002437.4:c.112G>C	NP_002428.1:p.Val38Leu
XM_005264326.2:c.112G>C	XP_005264383.1:p.Val38Leu
XM_005264327.2:c.-48G>C	XP_005264384.1:n.-48G>C
XM_006712021.2:c.64G>C	XP_006712084.1:p.Val22Leu
XM_005264326.4:c.112G>C	XP_005264383.1:p.Val38Leu
XM_006712021.3:c.64G>C	XP_006712084.1:p.Val22Leu
XM_017004150.1:c.94G>C	XP_016859639.1:p.Val32Leu
XM_017004151.1:c.64G>C	XP_016859640.1:p.Val22Leu
XM_017004152.1:c.-48G>C	XP_016859641.1:n.-48G>C
XM_024452913.1:c.64G>C	XP_024308681.1:p.Val22Leu
NM_002437.5:c.112G>C MANE Select	NP_002428.1:p.Val38Leu