Canonical Allele Identifier: CA494925808

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102467A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091146A>G , CM000678.2:g.31091146A>G	GRCh38
NC_000016.9:g.31102467A>G , CM000678.1:g.31102467A>G	GRCh37
NC_000016.8:g.31009968A>G	NCBI36
NG_011564.1:g.8810T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.480T>C MANE Select	ENSP00000378426.2:p.Ala160=
ENST00000300851.10:c.*91T>C	ENSP00000300851.6:n.*91T>C
ENST00000319788.11:c.*91T>C	ENSP00000326135.7:n.*91T>C
ENST00000354895.4:c.*91T>C	ENSP00000346969.4:n.*91T>C
ENST00000394971.7:c.*91T>C	ENSP00000378422.3:n.*91T>C
ENST00000394975.2:c.480T>C	ENSP00000378426.2:p.Ala160=
ENST00000420057.2:c.442T>C
ENST00000529564.1:c.283+2166T>C	ENSP00000431371.1:n.283+2166T>C
ENST00000532364.1:c.173+3411T>C	ENSP00000460316.1:n.173+3411T>C
ENST00000533518.5:c.353T>C
NM_001311311.1:c.564T>C	NP_001298240.1:p.Ala188=
NM_024006.4:c.480T>C	NP_076869.1:p.Ala160=
NM_024006.5:c.480T>C	NP_076869.1:p.Ala160=
NM_206824.1:c.*91T>C	NP_996560.1:n.*91T>C
NM_206824.2:c.*91T>C	NP_996560.1:n.*91T>C
XM_011545944.1:c.480T>C	XP_011544246.1:p.Ala160=
XM_011545945.1:c.*91T>C	XP_011544247.1:n.*91T>C
XR_950848.1:n.1268T>C
NM_024006.6:c.480T>C MANE Select	NP_076869.1:p.Ala160=
NM_001311311.2:c.564T>C	NP_001298240.1:p.Ala188=
NM_206824.3:c.*91T>C	NP_996560.1:n.*91T>C