Canonical Allele Identifier: CA2806498209

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090889C>A , CM000678.2:g.31090889C>A	GRCh38
NC_000016.9:g.31102210C>A , CM000678.1:g.31102210C>A	GRCh37
NC_000016.8:g.31009711C>A	NCBI36
NG_011564.1:g.9067G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*245G>T MANE Select	ENSP00000378426.2:n.*245G>T
ENST00000300851.10:c.*348G>T	ENSP00000300851.6:n.*348G>T
ENST00000319788.11:c.*348G>T	ENSP00000326135.7:n.*348G>T
ENST00000354895.4:c.*348G>T	ENSP00000346969.4:n.*348G>T
ENST00000394975.2:c.*245G>T	ENSP00000378426.2:n.*245G>T
ENST00000420057.2:c.699G>T
ENST00000529564.1:c.283+2423G>T	ENSP00000431371.1:n.283+2423G>T
ENST00000532364.1:c.173+3668G>T	ENSP00000460316.1:n.173+3668G>T
ENST00000533518.5:c.407+203G>T
NM_001311311.1:c.*245G>T	NP_001298240.1:n.*245G>T
NM_024006.4:c.*245G>T	NP_076869.1:n.*245G>T
NM_024006.5:c.*245G>T	NP_076869.1:n.*245G>T
NM_206824.1:c.*348G>T	NP_996560.1:n.*348G>T
NM_206824.2:c.*348G>T	NP_996560.1:n.*348G>T
XM_011545944.1:c.*245G>T	XP_011544246.1:n.*245G>T
XM_011545945.1:c.*348G>T	XP_011544247.1:n.*348G>T
XR_950848.1:n.1525G>T
NM_024006.6:c.*245G>T MANE Select	NP_076869.1:n.*245G>T
NM_001311311.2:c.*245G>T	NP_001298240.1:n.*245G>T
NM_206824.3:c.*348G>T	NP_996560.1:n.*348G>T