Canonical Allele Identifier: CA346207223

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27534795T>C (hg19) ; chr2:g.27311927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27311927T>C , CM000664.2:g.27311927T>C	GRCh38
NC_000002.11:g.27534795T>C , CM000664.1:g.27534795T>C	GRCh37
NC_000002.10:g.27388299T>C	NCBI36
NG_008075.1:g.15637A>G
NG_033055.1:g.1336A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.433A>G MANE Select	ENSP00000369383.1:p.Asn145Asp
ENST00000233545.6:c.433A>G	ENSP00000233545.2:p.Asn145Asp
ENST00000357186.10:c.265A>G	ENSP00000349713.6:p.Asn89Asp
ENST00000380044.5:c.433A>G	ENSP00000369383.1:p.Asn145Asp
ENST00000402310.5:c.408+287A>G	ENSP00000383955.1:n.408+287A>G
ENST00000402722.5:c.*40+567A>G	ENSP00000386000.1:n.*40+567A>G
ENST00000403262.6:c.433A>G	ENSP00000385671.1:p.Asn145Asp
ENST00000405076.5:c.244A>G	ENSP00000385175.1:p.Asn82Asp
ENST00000405983.5:c.478A>G	ENSP00000384586.1:p.Asn160Asp
ENST00000415514.5:c.*234A>G	ENSP00000388043.1:n.*234A>G
ENST00000426513.6:c.*98A>G	ENSP00000403824.2:n.*98A>G
ENST00000430991.5:c.267A>G
ENST00000616707.1:n.1461A>G
ENST00000620797.4:n.106A>G
ENST00000621183.4:n.736A>G
NM_002437.4:c.433A>G	NP_002428.1:p.Asn145Asp
XM_005264326.2:c.433A>G	XP_005264383.1:p.Asn145Asp
XM_005264327.2:c.274A>G	XP_005264384.1:p.Asn92Asp
XM_006712021.2:c.385A>G	XP_006712084.1:p.Asn129Asp
XM_005264326.4:c.433A>G	XP_005264383.1:p.Asn145Asp
XM_006712021.3:c.385A>G	XP_006712084.1:p.Asn129Asp
XM_017004150.1:c.415A>G	XP_016859639.1:p.Asn139Asp
XM_017004151.1:c.385A>G	XP_016859640.1:p.Asn129Asp
XM_017004152.1:c.274A>G	XP_016859641.1:p.Asn92Asp
XM_024452913.1:c.385A>G	XP_024308681.1:p.Asn129Asp
NM_002437.5:c.433A>G MANE Select	NP_002428.1:p.Asn145Asp