Canonical Allele Identifier: CA346205407

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532820A>T (hg19) ; chr2:g.27309952A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309952A>T , CM000664.2:g.27309952A>T	GRCh38
NC_000002.11:g.27532820A>T , CM000664.1:g.27532820A>T	GRCh37
NC_000002.10:g.27386324A>T	NCBI36
NG_008075.1:g.17612T>A
NG_033055.1:g.3311T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.491T>A MANE Select	ENSP00000369383.1:p.Ile164Asn
ENST00000233545.6:c.491T>A	ENSP00000233545.2:p.Ile164Asn
ENST00000357186.10:c.323T>A	ENSP00000349713.6:p.Ile108Asn
ENST00000380044.5:c.491T>A	ENSP00000369383.1:p.Ile164Asn
ENST00000402310.5:c.438T>A	ENSP00000383955.1:p.Tyr146Ter
ENST00000402722.5:c.*70T>A	ENSP00000386000.1:n.*70T>A
ENST00000405076.5:c.302T>A	ENSP00000385175.1:p.Ile101Asn
ENST00000405983.5:c.536T>A	ENSP00000384586.1:p.Ile179Asn
ENST00000415514.5:c.*292T>A	ENSP00000388043.1:n.*292T>A
ENST00000426513.6:c.*156T>A	ENSP00000403824.2:n.*156T>A
ENST00000430991.5:c.325T>A
ENST00000620797.4:n.164T>A
ENST00000621183.4:n.794T>A
NM_002437.4:c.491T>A	NP_002428.1:p.Ile164Asn
XM_005264326.2:c.491T>A	XP_005264383.1:p.Ile164Asn
XM_005264327.2:c.332T>A	XP_005264384.1:p.Ile111Asn
XM_006712021.2:c.443T>A	XP_006712084.1:p.Ile148Asn
XM_005264326.4:c.491T>A	XP_005264383.1:p.Ile164Asn
XM_006712021.3:c.443T>A	XP_006712084.1:p.Ile148Asn
XM_017004150.1:c.473T>A	XP_016859639.1:p.Ile158Asn
XM_017004151.1:c.443T>A	XP_016859640.1:p.Ile148Asn
XM_017004152.1:c.332T>A	XP_016859641.1:p.Ile111Asn
XM_024452913.1:c.443T>A	XP_024308681.1:p.Ile148Asn
NM_002437.5:c.491T>A MANE Select	NP_002428.1:p.Ile164Asn