Canonical Allele Identifier: CA1139664662

Gene: VKORC1

Linked Data

• ClinVar Variation Id: 887421
• ClinVar RCV Id: RCV001120143
• dbSNP Id: rs2057284100

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090962A>T , CM000678.2:g.31090962A>T	GRCh38
NC_000016.9:g.31102283A>T , CM000678.1:g.31102283A>T	GRCh37
NC_000016.8:g.31009784A>T	NCBI36
NG_011564.1:g.8994T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*172T>A MANE Select	ENSP00000378426.2:n.*172T>A
ENST00000300851.10:c.*275T>A	ENSP00000300851.6:n.*275T>A
ENST00000319788.11:c.*275T>A	ENSP00000326135.7:n.*275T>A
ENST00000354895.4:c.*275T>A	ENSP00000346969.4:n.*275T>A
ENST00000394975.2:c.*172T>A	ENSP00000378426.2:n.*172T>A
ENST00000420057.2:c.626T>A
ENST00000529564.1:c.283+2350T>A	ENSP00000431371.1:n.283+2350T>A
ENST00000532364.1:c.173+3595T>A	ENSP00000460316.1:n.173+3595T>A
ENST00000533518.5:c.407+130T>A
NM_001311311.1:c.*172T>A	NP_001298240.1:n.*172T>A
NM_024006.4:c.*172T>A	NP_076869.1:n.*172T>A
NM_024006.5:c.*172T>A	NP_076869.1:n.*172T>A
NM_206824.1:c.*275T>A	NP_996560.1:n.*275T>A
NM_206824.2:c.*275T>A	NP_996560.1:n.*275T>A
XM_011545944.1:c.*172T>A	XP_011544246.1:n.*172T>A
XM_011545945.1:c.*275T>A	XP_011544247.1:n.*275T>A
XR_950848.1:n.1452T>A
NM_024006.6:c.*172T>A MANE Select	NP_076869.1:n.*172T>A
NM_001311311.2:c.*172T>A	NP_001298240.1:n.*172T>A
NM_206824.3:c.*275T>A	NP_996560.1:n.*275T>A