Canonical Allele Identifier: CA2216888822

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091065A= , CM000678.2:g.31091065A=	GRCh38
NC_000016.9:g.31102386A= , CM000678.1:g.31102386A=	GRCh37
NC_000016.8:g.31009887A=	NCBI36
NG_011564.1:g.8891T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*69T= MANE Select	ENSP00000378426.2:n.*69T=
ENST00000300851.10:c.*172T=	ENSP00000300851.6:n.*172T=
ENST00000319788.11:c.*172T=	ENSP00000326135.7:n.*172T=
ENST00000354895.4:c.*172T=	ENSP00000346969.4:n.*172T=
ENST00000394975.2:c.*69T=	ENSP00000378426.2:n.*69T=
ENST00000420057.2:c.523T=
ENST00000529564.1:c.283+2247T=	ENSP00000431371.1:n.283+2247T=
ENST00000532364.1:c.173+3492T=	ENSP00000460316.1:n.173+3492T=
ENST00000533518.5:c.407+27T=
NM_001311311.1:c.*69T=	NP_001298240.1:n.*69T=
NM_024006.4:c.*69T=	NP_076869.1:n.*69T=
NM_024006.5:c.*69T=	NP_076869.1:n.*69T=
NM_206824.1:c.*172T=	NP_996560.1:n.*172T=
NM_206824.2:c.*172T=	NP_996560.1:n.*172T=
XM_011545944.1:c.*69T=	XP_011544246.1:n.*69T=
XM_011545945.1:c.*172T=	XP_011544247.1:n.*172T=
XR_950848.1:n.1349T=
NM_024006.6:c.*69T= MANE Select	NP_076869.1:n.*69T=
NM_001311311.2:c.*69T=	NP_001298240.1:n.*69T=
NM_206824.3:c.*172T=	NP_996560.1:n.*172T=