Canonical Allele Identifier: CA346205427

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532827C>G (hg19) ; chr2:g.27309959C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309959C>G , CM000664.2:g.27309959C>G	GRCh38
NC_000002.11:g.27532827C>G , CM000664.1:g.27532827C>G	GRCh37
NC_000002.10:g.27386331C>G	NCBI36
NG_008075.1:g.17605G>C
NG_033055.1:g.3304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.484G>C MANE Select	ENSP00000369383.1:p.Ala162Pro
ENST00000233545.6:c.484G>C	ENSP00000233545.2:p.Ala162Pro
ENST00000357186.10:c.316G>C	ENSP00000349713.6:p.Ala106Pro
ENST00000380044.5:c.484G>C	ENSP00000369383.1:p.Ala162Pro
ENST00000402310.5:c.431G>C	ENSP00000383955.1:p.Cys144Ser
ENST00000402722.5:c.*63G>C	ENSP00000386000.1:n.*63G>C
ENST00000405076.5:c.295G>C	ENSP00000385175.1:p.Ala99Pro
ENST00000405983.5:c.529G>C	ENSP00000384586.1:p.Ala177Pro
ENST00000415514.5:c.*285G>C	ENSP00000388043.1:n.*285G>C
ENST00000426513.6:c.*149G>C	ENSP00000403824.2:n.*149G>C
ENST00000430991.5:c.318G>C
ENST00000620797.4:n.157G>C
ENST00000621183.4:n.787G>C
NM_002437.4:c.484G>C	NP_002428.1:p.Ala162Pro
XM_005264326.2:c.484G>C	XP_005264383.1:p.Ala162Pro
XM_005264327.2:c.325G>C	XP_005264384.1:p.Ala109Pro
XM_006712021.2:c.436G>C	XP_006712084.1:p.Ala146Pro
XM_005264326.4:c.484G>C	XP_005264383.1:p.Ala162Pro
XM_006712021.3:c.436G>C	XP_006712084.1:p.Ala146Pro
XM_017004150.1:c.466G>C	XP_016859639.1:p.Ala156Pro
XM_017004151.1:c.436G>C	XP_016859640.1:p.Ala146Pro
XM_017004152.1:c.325G>C	XP_016859641.1:p.Ala109Pro
XM_024452913.1:c.436G>C	XP_024308681.1:p.Ala146Pro
NM_002437.5:c.484G>C MANE Select	NP_002428.1:p.Ala162Pro