Canonical Allele Identifier: CA2216888623

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090961_31090963delinsAAG , CM000678.2:g.31090961_31090963delinsAAG	GRCh38
NC_000016.9:g.31102282_31102284delinsAAG , CM000678.1:g.31102282_31102284delinsAAG	GRCh37
NC_000016.8:g.31009783_31009785delinsAAG	NCBI36
NG_011564.1:g.8993_8995delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*171_*173delinsCTT MANE Select	ENSP00000378426.2:n.*171_*173delinsCTT
ENST00000300851.10:c.*274_*276delinsCTT	ENSP00000300851.6:n.*274_*276delinsCTT
ENST00000319788.11:c.*274_*276delinsCTT	ENSP00000326135.7:n.*274_*276delinsCTT
ENST00000354895.4:c.*274_*276delinsCTT	ENSP00000346969.4:n.*274_*276delinsCTT
ENST00000394975.2:c.*171_*173delinsCTT	ENSP00000378426.2:n.*171_*173delinsCTT
ENST00000420057.2:c.625_627delinsCTT
ENST00000529564.1:c.283+2349_283+2351delinsCTT	ENSP00000431371.1:n.283+2349_283+2351delinsCTT
ENST00000532364.1:c.173+3594_173+3596delinsCTT	ENSP00000460316.1:n.173+3594_173+3596delinsCTT
ENST00000533518.5:c.407+129_407+131delinsCTT
NM_001311311.1:c.*171_*173delinsCTT	NP_001298240.1:n.*171_*173delinsCTT
NM_024006.4:c.*171_*173delinsCTT	NP_076869.1:n.*171_*173delinsCTT
NM_024006.5:c.*171_*173delinsCTT	NP_076869.1:n.*171_*173delinsCTT
NM_206824.1:c.*274_*276delinsCTT	NP_996560.1:n.*274_*276delinsCTT
NM_206824.2:c.*274_*276delinsCTT	NP_996560.1:n.*274_*276delinsCTT
XM_011545944.1:c.*171_*173delinsCTT	XP_011544246.1:n.*171_*173delinsCTT
XM_011545945.1:c.*274_*276delinsCTT	XP_011544247.1:n.*274_*276delinsCTT
XR_950848.1:n.1451_1453delinsCTT
NM_024006.6:c.*171_*173delinsCTT MANE Select	NP_076869.1:n.*171_*173delinsCTT
NM_001311311.2:c.*171_*173delinsCTT	NP_001298240.1:n.*171_*173delinsCTT
NM_206824.3:c.*274_*276delinsCTT	NP_996560.1:n.*274_*276delinsCTT