Canonical Allele Identifier: CA2216892865

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093816C= , CM000678.2:g.31093816C=	GRCh38
NC_000016.9:g.31105137C= , CM000678.1:g.31105137C=	GRCh37
NC_000016.8:g.31012638C=	NCBI36
NG_011564.1:g.6140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-395G= MANE Select	ENSP00000378426.2:n.174-395G=
ENST00000300851.10:c.174-334G=	ENSP00000300851.6:n.174-334G=
ENST00000319788.11:c.174-395G=	ENSP00000326135.7:n.174-395G=
ENST00000354895.4:c.173+741G=	ENSP00000346969.4:n.173+741G=
ENST00000394971.7:c.268-395G=	ENSP00000378422.3:n.268-395G=
ENST00000394975.2:c.174-395G=	ENSP00000378426.2:n.174-395G=
ENST00000420057.2:c.245+1573G=
ENST00000498155.1:c.271-395G=	ENSP00000417662.1:n.271-395G=
ENST00000529564.1:c.174-395G=	ENSP00000431371.1:n.174-395G=
ENST00000532364.1:c.173+741G=	ENSP00000460316.1:n.173+741G=
ENST00000533518.5:c.47-395G=
NM_001311311.1:c.174-395G=	NP_001298240.1:n.174-395G=
NM_024006.4:c.174-395G=	NP_076869.1:n.174-395G=
NM_024006.5:c.174-395G=	NP_076869.1:n.174-395G=
NM_206824.1:c.173+741G=	NP_996560.1:n.173+741G=
NM_206824.2:c.173+741G=	NP_996560.1:n.173+741G=
XM_011545944.1:c.174-395G=	XP_011544246.1:n.174-395G=
XM_011545945.1:c.173+741G=	XP_011544247.1:n.173+741G=
XR_950848.1:n.962-395G=
NM_024006.6:c.174-395G= MANE Select	NP_076869.1:n.174-395G=
NM_001311311.2:c.174-395G=	NP_001298240.1:n.174-395G=
NM_206824.3:c.173+741G=	NP_996560.1:n.173+741G=