Canonical Allele Identifier: CA395729821

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102602A>C (hg19) ; chr16:g.31091281A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091281A>C , CM000678.2:g.31091281A>C	GRCh38
NC_000016.9:g.31102602A>C , CM000678.1:g.31102602A>C	GRCh37
NC_000016.8:g.31010103A>C	NCBI36
NG_011564.1:g.8675T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.345T>G MANE Select	ENSP00000378426.2:p.Ala115=
ENST00000300851.10:c.406T>G	ENSP00000300851.6:p.Trp136Gly
ENST00000319788.11:c.427T>G	ENSP00000326135.7:p.Trp143Gly
ENST00000354895.4:c.235T>G	ENSP00000346969.4:p.Trp79Gly
ENST00000394971.7:c.439T>G	ENSP00000378422.3:p.Trp147Gly
ENST00000394975.2:c.345T>G	ENSP00000378426.2:p.Ala115=
ENST00000420057.2:c.307T>G
ENST00000472468.1:c.30T>G	ENSP00000458994.1:p.Ala10=
ENST00000498155.1:c.442T>G	ENSP00000417662.1:p.Trp148Gly
ENST00000529564.1:c.283+2031T>G	ENSP00000431371.1:n.283+2031T>G
ENST00000532364.1:c.173+3276T>G	ENSP00000460316.1:n.173+3276T>G
ENST00000533518.5:c.218T>G
NM_001311311.1:c.429T>G	NP_001298240.1:p.Ala143=
NM_024006.4:c.345T>G	NP_076869.1:p.Ala115=
NM_024006.5:c.345T>G	NP_076869.1:p.Ala115=
NM_206824.1:c.235T>G	NP_996560.1:p.Trp79Gly
NM_206824.2:c.235T>G	NP_996560.1:p.Trp79Gly
XM_011545944.1:c.345T>G	XP_011544246.1:p.Ala115=
XM_011545945.1:c.235T>G	XP_011544247.1:p.Trp79Gly
XR_950848.1:n.1133T>G
NM_024006.6:c.345T>G MANE Select	NP_076869.1:p.Ala115=
NM_001311311.2:c.429T>G	NP_001298240.1:p.Ala143=
NM_206824.3:c.235T>G	NP_996560.1:p.Trp79Gly