Canonical Allele Identifier: CA346209521

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535970A>G (hg19) ; chr2:g.27313103A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313103A>G , CM000664.2:g.27313103A>G	GRCh38
NC_000002.11:g.27535970A>G , CM000664.1:g.27535970A>G	GRCh37
NC_000002.10:g.27389474A>G	NCBI36
NG_008075.1:g.14462T>C
NG_033055.1:g.161T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.77T>C MANE Select	ENSP00000369383.1:p.Leu26Pro
ENST00000233545.6:c.77T>C	ENSP00000233545.2:p.Leu26Pro
ENST00000357186.10:c.19-331T>C	ENSP00000349713.6:n.19-331T>C
ENST00000380044.5:c.77T>C	ENSP00000369383.1:p.Leu26Pro
ENST00000402310.5:c.77T>C	ENSP00000383955.1:p.Leu26Pro
ENST00000402722.5:c.71-29T>C	ENSP00000386000.1:n.71-29T>C
ENST00000403262.6:c.77T>C	ENSP00000385671.1:p.Leu26Pro
ENST00000405076.5:c.77T>C	ENSP00000385175.1:p.Leu26Pro
ENST00000405983.5:c.122T>C	ENSP00000384586.1:p.Leu41Pro
ENST00000415514.5:c.228-331T>C	ENSP00000388043.1:n.228-331T>C
ENST00000426513.6:c.71-29T>C	ENSP00000403824.2:n.71-29T>C
ENST00000428910.5:c.-2T>C	ENSP00000405235.1:n.-2T>C
ENST00000430991.5:c.7T>C
ENST00000616446.1:n.54T>C
ENST00000616707.1:n.285T>C
ENST00000617583.4:n.103T>C
ENST00000621183.4:n.133T>C
ENST00000621470.4:n.122-29T>C
ENST00000622003.4:n.250T>C
NM_002437.4:c.77T>C	NP_002428.1:p.Leu26Pro
XM_005264326.2:c.77T>C	XP_005264383.1:p.Leu26Pro
XM_005264327.2:c.-54-29T>C	XP_005264384.1:n.-54-29T>C
XM_006712021.2:c.29T>C	XP_006712084.1:p.Leu10Pro
XM_005264326.4:c.77T>C	XP_005264383.1:p.Leu26Pro
XM_006712021.3:c.29T>C	XP_006712084.1:p.Leu10Pro
XM_017004150.1:c.59T>C	XP_016859639.1:p.Leu20Pro
XM_017004151.1:c.29T>C	XP_016859640.1:p.Leu10Pro
XM_017004152.1:c.-54-29T>C	XP_016859641.1:n.-54-29T>C
XM_024452913.1:c.29T>C	XP_024308681.1:p.Leu10Pro
NM_002437.5:c.77T>C MANE Select	NP_002428.1:p.Leu26Pro