Canonical Allele Identifier: CA395729630

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102559C>T (hg19) ; chr16:g.31091238C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091238C>T , CM000678.2:g.31091238C>T	GRCh38
NC_000016.9:g.31102559C>T , CM000678.1:g.31102559C>T	GRCh37
NC_000016.8:g.31010060C>T	NCBI36
NG_011564.1:g.8718G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.388G>A MANE Select	ENSP00000378426.2:p.Asp130Asn
ENST00000300851.10:c.449G>A	ENSP00000300851.6:p.Ter150=
ENST00000319788.11:c.470G>A	ENSP00000326135.7:p.Ter157=
ENST00000354895.4:c.278G>A	ENSP00000346969.4:p.Ter93=
ENST00000394971.7:c.482G>A	ENSP00000378422.3:p.Ter161=
ENST00000394975.2:c.388G>A	ENSP00000378426.2:p.Asp130Asn
ENST00000420057.2:c.350G>A
ENST00000472468.1:c.73G>A	ENSP00000458994.1:p.Asp25Asn
ENST00000498155.1:c.485G>A	ENSP00000417662.1:p.Ter162=
ENST00000529564.1:c.283+2074G>A	ENSP00000431371.1:n.283+2074G>A
ENST00000532364.1:c.173+3319G>A	ENSP00000460316.1:n.173+3319G>A
ENST00000533518.5:c.261G>A
NM_001311311.1:c.472G>A	NP_001298240.1:p.Asp158Asn
NM_024006.4:c.388G>A	NP_076869.1:p.Asp130Asn
NM_024006.5:c.388G>A	NP_076869.1:p.Asp130Asn
NM_206824.1:c.278G>A	NP_996560.1:p.Ter93=
NM_206824.2:c.278G>A	NP_996560.1:p.Ter93=
XM_011545944.1:c.388G>A	XP_011544246.1:p.Asp130Asn
XM_011545945.1:c.278G>A	XP_011544247.1:p.Ter93=
XR_950848.1:n.1176G>A
NM_024006.6:c.388G>A MANE Select	NP_076869.1:p.Asp130Asn
NM_001311311.2:c.472G>A	NP_001298240.1:p.Asp158Asn
NM_206824.3:c.278G>A	NP_996560.1:p.Ter93=