Canonical Allele Identifier: CA2216893127

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094011A= , CM000678.2:g.31094011A=	GRCh38
NC_000016.9:g.31105332A= , CM000678.1:g.31105332A=	GRCh37
NC_000016.8:g.31012833A=	NCBI36
NG_011564.1:g.5945T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.173+546T= MANE Select	ENSP00000378426.2:n.173+546T=
ENST00000300851.10:c.174-529T=	ENSP00000300851.6:n.174-529T=
ENST00000319788.11:c.173+546T=	ENSP00000326135.7:n.173+546T=
ENST00000354895.4:c.173+546T=	ENSP00000346969.4:n.173+546T=
ENST00000394971.7:c.267+224T=	ENSP00000378422.3:n.267+224T=
ENST00000394975.2:c.173+546T=	ENSP00000378426.2:n.173+546T=
ENST00000420057.2:c.245+1378T=
ENST00000498155.1:c.271-590T=	ENSP00000417662.1:n.271-590T=
ENST00000529564.1:c.173+546T=	ENSP00000431371.1:n.173+546T=
ENST00000532364.1:c.173+546T=	ENSP00000460316.1:n.173+546T=
ENST00000533518.5:c.46+546T=
NM_001311311.1:c.173+546T=	NP_001298240.1:n.173+546T=
NM_024006.4:c.173+546T=	NP_076869.1:n.173+546T=
NM_024006.5:c.173+546T=	NP_076869.1:n.173+546T=
NM_206824.1:c.173+546T=	NP_996560.1:n.173+546T=
NM_206824.2:c.173+546T=	NP_996560.1:n.173+546T=
XM_011545944.1:c.173+546T=	XP_011544246.1:n.173+546T=
XM_011545945.1:c.173+546T=	XP_011544247.1:n.173+546T=
XR_950848.1:n.961+546T=
NM_024006.6:c.173+546T= MANE Select	NP_076869.1:n.173+546T=
NM_001311311.2:c.173+546T=	NP_001298240.1:n.173+546T=
NM_206824.3:c.173+546T=	NP_996560.1:n.173+546T=