Canonical Allele Identifier: CA395730120

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102663C>G (hg19) ; chr16:g.31091342C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091342C>G , CM000678.2:g.31091342C>G	GRCh38
NC_000016.9:g.31102663C>G , CM000678.1:g.31102663C>G	GRCh37
NC_000016.8:g.31010164C>G	NCBI36
NG_011564.1:g.8614G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.284G>C MANE Select	ENSP00000378426.2:p.Gly95Ala
ENST00000300851.10:c.345G>C	ENSP00000300851.6:p.Arg115Ser
ENST00000319788.11:c.366G>C	ENSP00000326135.7:p.Ala122=
ENST00000354895.4:c.174G>C	ENSP00000346969.4:p.Arg58Ser
ENST00000394971.7:c.378G>C	ENSP00000378422.3:p.Arg126Ser
ENST00000394975.2:c.284G>C	ENSP00000378426.2:p.Gly95Ala
ENST00000420057.2:c.246G>C
ENST00000472468.1:c.-32G>C	ENSP00000458994.1:n.-32G>C
ENST00000498155.1:c.381G>C	ENSP00000417662.1:p.Arg127Ser
ENST00000529564.1:c.283+1970G>C	ENSP00000431371.1:n.283+1970G>C
ENST00000532364.1:c.173+3215G>C	ENSP00000460316.1:n.173+3215G>C
ENST00000533518.5:c.157G>C
NM_001311311.1:c.368G>C	NP_001298240.1:p.Arg123Pro
NM_024006.4:c.284G>C	NP_076869.1:p.Gly95Ala
NM_024006.5:c.284G>C	NP_076869.1:p.Gly95Ala
NM_206824.1:c.174G>C	NP_996560.1:p.Arg58Ser
NM_206824.2:c.174G>C	NP_996560.1:p.Arg58Ser
XM_011545944.1:c.284G>C	XP_011544246.1:p.Gly95Ala
XM_011545945.1:c.174G>C	XP_011544247.1:p.Arg58Ser
XR_950848.1:n.1072G>C
NM_024006.6:c.284G>C MANE Select	NP_076869.1:p.Gly95Ala
NM_001311311.2:c.368G>C	NP_001298240.1:p.Arg123Pro
NM_206824.3:c.174G>C	NP_996560.1:p.Arg58Ser