Canonical Allele Identifier: CA395729170

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102477T>C (hg19) ; chr16:g.31091156T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091156T>C , CM000678.2:g.31091156T>C	GRCh38
NC_000016.9:g.31102477T>C , CM000678.1:g.31102477T>C	GRCh37
NC_000016.8:g.31009978T>C	NCBI36
NG_011564.1:g.8800A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.470A>G MANE Select	ENSP00000378426.2:p.Gln157Arg
ENST00000300851.10:c.*81A>G	ENSP00000300851.6:n.*81A>G
ENST00000319788.11:c.*81A>G	ENSP00000326135.7:n.*81A>G
ENST00000354895.4:c.*81A>G	ENSP00000346969.4:n.*81A>G
ENST00000394971.7:c.*81A>G	ENSP00000378422.3:n.*81A>G
ENST00000394975.2:c.470A>G	ENSP00000378426.2:p.Gln157Arg
ENST00000420057.2:c.432A>G
ENST00000529564.1:c.283+2156A>G	ENSP00000431371.1:n.283+2156A>G
ENST00000532364.1:c.173+3401A>G	ENSP00000460316.1:n.173+3401A>G
ENST00000533518.5:c.343A>G
NM_001311311.1:c.554A>G	NP_001298240.1:p.Gln185Arg
NM_024006.4:c.470A>G	NP_076869.1:p.Gln157Arg
NM_024006.5:c.470A>G	NP_076869.1:p.Gln157Arg
NM_206824.1:c.*81A>G	NP_996560.1:n.*81A>G
NM_206824.2:c.*81A>G	NP_996560.1:n.*81A>G
XM_011545944.1:c.470A>G	XP_011544246.1:p.Gln157Arg
XM_011545945.1:c.*81A>G	XP_011544247.1:n.*81A>G
XR_950848.1:n.1258A>G
NM_024006.6:c.470A>G MANE Select	NP_076869.1:p.Gln157Arg
NM_001311311.2:c.554A>G	NP_001298240.1:p.Gln185Arg
NM_206824.3:c.*81A>G	NP_996560.1:n.*81A>G