Canonical Allele Identifier: CA395729657

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102565G>C (hg19) ; chr16:g.31091244G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091244G>C , CM000678.2:g.31091244G>C	GRCh38
NC_000016.9:g.31102565G>C , CM000678.1:g.31102565G>C	GRCh37
NC_000016.8:g.31010066G>C	NCBI36
NG_011564.1:g.8712C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.382C>G MANE Select	ENSP00000378426.2:p.Leu128Val
ENST00000300851.10:c.443C>G	ENSP00000300851.6:p.Ala148Gly
ENST00000319788.11:c.464C>G	ENSP00000326135.7:p.Ala155Gly
ENST00000354895.4:c.272C>G	ENSP00000346969.4:p.Ala91Gly
ENST00000394971.7:c.476C>G	ENSP00000378422.3:p.Ala159Gly
ENST00000394975.2:c.382C>G	ENSP00000378426.2:p.Leu128Val
ENST00000420057.2:c.344C>G
ENST00000472468.1:c.67C>G	ENSP00000458994.1:p.Leu23Val
ENST00000498155.1:c.479C>G	ENSP00000417662.1:p.Ala160Gly
ENST00000529564.1:c.283+2068C>G	ENSP00000431371.1:n.283+2068C>G
ENST00000532364.1:c.173+3313C>G	ENSP00000460316.1:n.173+3313C>G
ENST00000533518.5:c.255C>G
NM_001311311.1:c.466C>G	NP_001298240.1:p.Leu156Val
NM_024006.4:c.382C>G	NP_076869.1:p.Leu128Val
NM_024006.5:c.382C>G	NP_076869.1:p.Leu128Val
NM_206824.1:c.272C>G	NP_996560.1:p.Ala91Gly
NM_206824.2:c.272C>G	NP_996560.1:p.Ala91Gly
XM_011545944.1:c.382C>G	XP_011544246.1:p.Leu128Val
XM_011545945.1:c.272C>G	XP_011544247.1:p.Ala91Gly
XR_950848.1:n.1170C>G
NM_024006.6:c.382C>G MANE Select	NP_076869.1:p.Leu128Val
NM_001311311.2:c.466C>G	NP_001298240.1:p.Leu156Val
NM_206824.3:c.272C>G	NP_996560.1:p.Ala91Gly