Canonical Allele Identifier: CA280619650

Gene: VKORC1

Linked Data

• dbSNP Id: rs767194687
• MyVariant Identifiers: chr16:g.31102248_31102249insA (hg19) ; chr16:g.31090927_31090928insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090928dup , CM000678.2:g.31090928dup	GRCh38
NC_000016.9:g.31102249dup , CM000678.1:g.31102249dup	GRCh37
NC_000016.8:g.31009750dup	NCBI36
NG_011564.1:g.9028dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.*206dup MANE Select	ENSP00000378426.2:n.*206dup
ENST00000300851.10:c.*309dup	ENSP00000300851.6:n.*309dup
ENST00000319788.11:c.*309dup	ENSP00000326135.7:n.*309dup
ENST00000354895.4:c.*309dup	ENSP00000346969.4:n.*309dup
ENST00000394975.2:c.*206dup	ENSP00000378426.2:n.*206dup
ENST00000420057.2:c.660dup
ENST00000529564.1:c.283+2384dup	ENSP00000431371.1:n.283+2384dup
ENST00000532364.1:c.173+3629dup	ENSP00000460316.1:n.173+3629dup
ENST00000533518.5:c.407+164dup
NM_001311311.1:c.*206dup	NP_001298240.1:n.*206dup
NM_024006.4:c.*206dup	NP_076869.1:n.*206dup
NM_024006.5:c.*206dup	NP_076869.1:n.*206dup
NM_206824.1:c.*309dup	NP_996560.1:n.*309dup
NM_206824.2:c.*309dup	NP_996560.1:n.*309dup
XM_011545944.1:c.*206dup	XP_011544246.1:n.*206dup
XM_011545945.1:c.*309dup	XP_011544247.1:n.*309dup
XR_950848.1:n.1486dup
NM_024006.6:c.*206dup MANE Select	NP_076869.1:n.*206dup
NM_001311311.2:c.*206dup	NP_001298240.1:n.*206dup
NM_206824.3:c.*309dup	NP_996560.1:n.*309dup