Canonical Allele Identifier: CA395729413

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102516C>G (hg19) ; chr16:g.31091195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091195C>G , CM000678.2:g.31091195C>G	GRCh38
NC_000016.9:g.31102516C>G , CM000678.1:g.31102516C>G	GRCh37
NC_000016.8:g.31010017C>G	NCBI36
NG_011564.1:g.8761G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.431G>C MANE Select	ENSP00000378426.2:p.Ser144Thr
ENST00000300851.10:c.*42G>C	ENSP00000300851.6:n.*42G>C
ENST00000319788.11:c.*42G>C	ENSP00000326135.7:n.*42G>C
ENST00000354895.4:c.*42G>C	ENSP00000346969.4:n.*42G>C
ENST00000394971.7:c.*42G>C	ENSP00000378422.3:n.*42G>C
ENST00000394975.2:c.431G>C	ENSP00000378426.2:p.Ser144Thr
ENST00000420057.2:c.393G>C
ENST00000472468.1:c.116G>C	ENSP00000458994.1:p.Ser39Thr
ENST00000498155.1:c.*42G>C	ENSP00000417662.1:n.*42G>C
ENST00000529564.1:c.283+2117G>C	ENSP00000431371.1:n.283+2117G>C
ENST00000532364.1:c.173+3362G>C	ENSP00000460316.1:n.173+3362G>C
ENST00000533518.5:c.304G>C
NM_001311311.1:c.515G>C	NP_001298240.1:p.Ser172Thr
NM_024006.4:c.431G>C	NP_076869.1:p.Ser144Thr
NM_024006.5:c.431G>C	NP_076869.1:p.Ser144Thr
NM_206824.1:c.*42G>C	NP_996560.1:n.*42G>C
NM_206824.2:c.*42G>C	NP_996560.1:n.*42G>C
XM_011545944.1:c.431G>C	XP_011544246.1:p.Ser144Thr
XM_011545945.1:c.*42G>C	XP_011544247.1:n.*42G>C
XR_950848.1:n.1219G>C
NM_024006.6:c.431G>C MANE Select	NP_076869.1:p.Ser144Thr
NM_001311311.2:c.515G>C	NP_001298240.1:p.Ser172Thr
NM_206824.3:c.*42G>C	NP_996560.1:n.*42G>C