Canonical Allele Identifier: CA395729735

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102583A>T (hg19) ; chr16:g.31091262A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091262A>T , CM000678.2:g.31091262A>T	GRCh38
NC_000016.9:g.31102583A>T , CM000678.1:g.31102583A>T	GRCh37
NC_000016.8:g.31010084A>T	NCBI36
NG_011564.1:g.8694T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.364T>A MANE Select	ENSP00000378426.2:p.Trp122Arg
ENST00000300851.10:c.425T>A	ENSP00000300851.6:p.Leu142Gln
ENST00000319788.11:c.446T>A	ENSP00000326135.7:p.Leu149Gln
ENST00000354895.4:c.254T>A	ENSP00000346969.4:p.Leu85Gln
ENST00000394971.7:c.458T>A	ENSP00000378422.3:p.Leu153Gln
ENST00000394975.2:c.364T>A	ENSP00000378426.2:p.Trp122Arg
ENST00000420057.2:c.326T>A
ENST00000472468.1:c.49T>A	ENSP00000458994.1:p.Trp17Arg
ENST00000498155.1:c.461T>A	ENSP00000417662.1:p.Leu154Gln
ENST00000529564.1:c.283+2050T>A	ENSP00000431371.1:n.283+2050T>A
ENST00000532364.1:c.173+3295T>A	ENSP00000460316.1:n.173+3295T>A
ENST00000533518.5:c.237T>A
NM_001311311.1:c.448T>A	NP_001298240.1:p.Trp150Arg
NM_024006.4:c.364T>A	NP_076869.1:p.Trp122Arg
NM_024006.5:c.364T>A	NP_076869.1:p.Trp122Arg
NM_206824.1:c.254T>A	NP_996560.1:p.Leu85Gln
NM_206824.2:c.254T>A	NP_996560.1:p.Leu85Gln
XM_011545944.1:c.364T>A	XP_011544246.1:p.Trp122Arg
XM_011545945.1:c.254T>A	XP_011544247.1:p.Leu85Gln
XR_950848.1:n.1152T>A
NM_024006.6:c.364T>A MANE Select	NP_076869.1:p.Trp122Arg
NM_001311311.2:c.448T>A	NP_001298240.1:p.Trp150Arg
NM_206824.3:c.254T>A	NP_996560.1:p.Leu85Gln