Canonical Allele Identifier: CA395729662

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102566C>T (hg19) ; chr16:g.31091245C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091245C>T , CM000678.2:g.31091245C>T	GRCh38
NC_000016.9:g.31102566C>T , CM000678.1:g.31102566C>T	GRCh37
NC_000016.8:g.31010067C>T	NCBI36
NG_011564.1:g.8711G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.381G>A MANE Select	ENSP00000378426.2:p.Val127=
ENST00000300851.10:c.442G>A	ENSP00000300851.6:p.Ala148Thr
ENST00000319788.11:c.463G>A	ENSP00000326135.7:p.Ala155Thr
ENST00000354895.4:c.271G>A	ENSP00000346969.4:p.Ala91Thr
ENST00000394971.7:c.475G>A	ENSP00000378422.3:p.Ala159Thr
ENST00000394975.2:c.381G>A	ENSP00000378426.2:p.Val127=
ENST00000420057.2:c.343G>A
ENST00000472468.1:c.66G>A	ENSP00000458994.1:p.Val22=
ENST00000498155.1:c.478G>A	ENSP00000417662.1:p.Ala160Thr
ENST00000529564.1:c.283+2067G>A	ENSP00000431371.1:n.283+2067G>A
ENST00000532364.1:c.173+3312G>A	ENSP00000460316.1:n.173+3312G>A
ENST00000533518.5:c.254G>A
NM_001311311.1:c.465G>A	NP_001298240.1:p.Val155=
NM_024006.4:c.381G>A	NP_076869.1:p.Val127=
NM_024006.5:c.381G>A	NP_076869.1:p.Val127=
NM_206824.1:c.271G>A	NP_996560.1:p.Ala91Thr
NM_206824.2:c.271G>A	NP_996560.1:p.Ala91Thr
XM_011545944.1:c.381G>A	XP_011544246.1:p.Val127=
XM_011545945.1:c.271G>A	XP_011544247.1:p.Ala91Thr
XR_950848.1:n.1169G>A
NM_024006.6:c.381G>A MANE Select	NP_076869.1:p.Val127=
NM_001311311.2:c.465G>A	NP_001298240.1:p.Val155=
NM_206824.3:c.271G>A	NP_996560.1:p.Ala91Thr