Canonical Allele Identifier: CA2216888618

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090960_31090963delinsAAAG , CM000678.2:g.31090960_31090963delinsAAAG	GRCh38
NC_000016.9:g.31102281_31102284delinsAAAG , CM000678.1:g.31102281_31102284delinsAAAG	GRCh37
NC_000016.8:g.31009782_31009785delinsAAAG	NCBI36
NG_011564.1:g.8993_8996delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*171_*174delinsCTTT MANE Select	ENSP00000378426.2:n.*171_*174delinsCTTT
ENST00000300851.10:c.*274_*277delinsCTTT	ENSP00000300851.6:n.*274_*277delinsCTTT
ENST00000319788.11:c.*274_*277delinsCTTT	ENSP00000326135.7:n.*274_*277delinsCTTT
ENST00000354895.4:c.*274_*277delinsCTTT	ENSP00000346969.4:n.*274_*277delinsCTTT
ENST00000394975.2:c.*171_*174delinsCTTT	ENSP00000378426.2:n.*171_*174delinsCTTT
ENST00000420057.2:c.625_628delinsCTTT
ENST00000529564.1:c.283+2349_283+2352delinsCTTT	ENSP00000431371.1:n.283+2349_283+2352delinsCTTT
ENST00000532364.1:c.173+3594_173+3597delinsCTTT	ENSP00000460316.1:n.173+3594_173+3597delinsCTTT
ENST00000533518.5:c.407+129_407+132delinsCTTT
NM_001311311.1:c.*171_*174delinsCTTT	NP_001298240.1:n.*171_*174delinsCTTT
NM_024006.4:c.*171_*174delinsCTTT	NP_076869.1:n.*171_*174delinsCTTT
NM_024006.5:c.*171_*174delinsCTTT	NP_076869.1:n.*171_*174delinsCTTT
NM_206824.1:c.*274_*277delinsCTTT	NP_996560.1:n.*274_*277delinsCTTT
NM_206824.2:c.*274_*277delinsCTTT	NP_996560.1:n.*274_*277delinsCTTT
XM_011545944.1:c.*171_*174delinsCTTT	XP_011544246.1:n.*171_*174delinsCTTT
XM_011545945.1:c.*274_*277delinsCTTT	XP_011544247.1:n.*274_*277delinsCTTT
XR_950848.1:n.1451_1454delinsCTTT
NM_024006.6:c.*171_*174delinsCTTT MANE Select	NP_076869.1:n.*171_*174delinsCTTT
NM_001311311.2:c.*171_*174delinsCTTT	NP_001298240.1:n.*171_*174delinsCTTT
NM_206824.3:c.*274_*277delinsCTTT	NP_996560.1:n.*274_*277delinsCTTT