Canonical Allele Identifier: CA494925804

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102464C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091143C>T , CM000678.2:g.31091143C>T	GRCh38
NC_000016.9:g.31102464C>T , CM000678.1:g.31102464C>T	GRCh37
NC_000016.8:g.31009965C>T	NCBI36
NG_011564.1:g.8813G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.483G>A MANE Select	ENSP00000378426.2:p.Lys161=
ENST00000300851.10:c.*94G>A	ENSP00000300851.6:n.*94G>A
ENST00000319788.11:c.*94G>A	ENSP00000326135.7:n.*94G>A
ENST00000354895.4:c.*94G>A	ENSP00000346969.4:n.*94G>A
ENST00000394971.7:c.*94G>A	ENSP00000378422.3:n.*94G>A
ENST00000394975.2:c.483G>A	ENSP00000378426.2:p.Lys161=
ENST00000420057.2:c.445G>A
ENST00000529564.1:c.283+2169G>A	ENSP00000431371.1:n.283+2169G>A
ENST00000532364.1:c.173+3414G>A	ENSP00000460316.1:n.173+3414G>A
ENST00000533518.5:c.356G>A
NM_001311311.1:c.567G>A	NP_001298240.1:p.Lys189=
NM_024006.4:c.483G>A	NP_076869.1:p.Lys161=
NM_024006.5:c.483G>A	NP_076869.1:p.Lys161=
NM_206824.1:c.*94G>A	NP_996560.1:n.*94G>A
NM_206824.2:c.*94G>A	NP_996560.1:n.*94G>A
XM_011545944.1:c.483G>A	XP_011544246.1:p.Lys161=
XM_011545945.1:c.*94G>A	XP_011544247.1:n.*94G>A
XR_950848.1:n.1271G>A
NM_024006.6:c.483G>A MANE Select	NP_076869.1:p.Lys161=
NM_001311311.2:c.567G>A	NP_001298240.1:p.Lys189=
NM_206824.3:c.*94G>A	NP_996560.1:n.*94G>A