Canonical Allele Identifier: CA395730056

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102649G>T (hg19) ; chr16:g.31091328G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091328G>T , CM000678.2:g.31091328G>T	GRCh38
NC_000016.9:g.31102649G>T , CM000678.1:g.31102649G>T	GRCh37
NC_000016.8:g.31010150G>T	NCBI36
NG_011564.1:g.8628C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.298C>A MANE Select	ENSP00000378426.2:p.Arg100Ser
ENST00000300851.10:c.359C>A	ENSP00000300851.6:p.Thr120Lys
ENST00000319788.11:c.380C>A	ENSP00000326135.7:p.Thr127Lys
ENST00000354895.4:c.188C>A	ENSP00000346969.4:p.Thr63Lys
ENST00000394971.7:c.392C>A	ENSP00000378422.3:p.Thr131Lys
ENST00000394975.2:c.298C>A	ENSP00000378426.2:p.Arg100Ser
ENST00000420057.2:c.260C>A
ENST00000472468.1:c.-18C>A	ENSP00000458994.1:n.-18C>A
ENST00000498155.1:c.395C>A	ENSP00000417662.1:p.Thr132Lys
ENST00000529564.1:c.283+1984C>A	ENSP00000431371.1:n.283+1984C>A
ENST00000532364.1:c.173+3229C>A	ENSP00000460316.1:n.173+3229C>A
ENST00000533518.5:c.171C>A
NM_001311311.1:c.382C>A	NP_001298240.1:p.Arg128Ser
NM_024006.4:c.298C>A	NP_076869.1:p.Arg100Ser
NM_024006.5:c.298C>A	NP_076869.1:p.Arg100Ser
NM_206824.1:c.188C>A	NP_996560.1:p.Thr63Lys
NM_206824.2:c.188C>A	NP_996560.1:p.Thr63Lys
XM_011545944.1:c.298C>A	XP_011544246.1:p.Arg100Ser
XM_011545945.1:c.188C>A	XP_011544247.1:p.Thr63Lys
XR_950848.1:n.1086C>A
NM_024006.6:c.298C>A MANE Select	NP_076869.1:p.Arg100Ser
NM_001311311.2:c.382C>A	NP_001298240.1:p.Arg128Ser
NM_206824.3:c.188C>A	NP_996560.1:p.Thr63Lys