Canonical Allele Identifier: CA346207927

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535387G>A (hg19) ; chr2:g.27312520G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312520G>A , CM000664.2:g.27312520G>A	GRCh38
NC_000002.11:g.27535387G>A , CM000664.1:g.27535387G>A	GRCh37
NC_000002.10:g.27388891G>A	NCBI36
NG_008075.1:g.15045C>T
NG_033055.1:g.744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.349C>T MANE Select	ENSP00000369383.1:p.Gln117Ter
ENST00000233545.6:c.349C>T	ENSP00000233545.2:p.Gln117Ter
ENST00000357186.10:c.181C>T	ENSP00000349713.6:p.Gln61Ter
ENST00000380044.5:c.349C>T	ENSP00000369383.1:p.Gln117Ter
ENST00000402310.5:c.349C>T	ENSP00000383955.1:p.Gln117Ter
ENST00000402722.5:c.*14C>T	ENSP00000386000.1:n.*14C>T
ENST00000403262.6:c.349C>T	ENSP00000385671.1:p.Gln117Ter
ENST00000405076.5:c.187-274C>T	ENSP00000385175.1:n.187-274C>T
ENST00000405983.5:c.394C>T	ENSP00000384586.1:p.Gln132Ter
ENST00000415514.5:c.*150C>T	ENSP00000388043.1:n.*150C>T
ENST00000426513.6:c.*14C>T	ENSP00000403824.2:n.*14C>T
ENST00000428910.5:c.271C>T	ENSP00000405235.1:p.Gln91Ter
ENST00000430991.5:c.209+160C>T
ENST00000475085.1:n.377C>T
ENST00000616446.1:n.326C>T
ENST00000616707.1:n.868C>T
ENST00000617583.4:n.375C>T
ENST00000621183.4:n.405C>T
ENST00000621470.4:n.365C>T
ENST00000622003.4:n.522C>T
NM_002437.4:c.349C>T	NP_002428.1:p.Gln117Ter
XM_005264326.2:c.349C>T	XP_005264383.1:p.Gln117Ter
XM_005264327.2:c.190C>T	XP_005264384.1:p.Gln64Ter
XM_006712021.2:c.301C>T	XP_006712084.1:p.Gln101Ter
XM_005264326.4:c.349C>T	XP_005264383.1:p.Gln117Ter
XM_006712021.3:c.301C>T	XP_006712084.1:p.Gln101Ter
XM_017004150.1:c.331C>T	XP_016859639.1:p.Gln111Ter
XM_017004151.1:c.301C>T	XP_016859640.1:p.Gln101Ter
XM_017004152.1:c.190C>T	XP_016859641.1:p.Gln64Ter
XM_024452913.1:c.301C>T	XP_024308681.1:p.Gln101Ter
NM_002437.5:c.349C>T MANE Select	NP_002428.1:p.Gln117Ter