Canonical Allele Identifier: CA395729979

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102633A>C (hg19) ; chr16:g.31091312A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091312A>C , CM000678.2:g.31091312A>C	GRCh38
NC_000016.9:g.31102633A>C , CM000678.1:g.31102633A>C	GRCh37
NC_000016.8:g.31010134A>C	NCBI36
NG_011564.1:g.8644T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.314T>G MANE Select	ENSP00000378426.2:p.Leu105Arg
ENST00000300851.10:c.375T>G	ENSP00000300851.6:p.Pro125=
ENST00000319788.11:c.396T>G	ENSP00000326135.7:p.Pro132=
ENST00000354895.4:c.204T>G	ENSP00000346969.4:p.Pro68=
ENST00000394971.7:c.408T>G	ENSP00000378422.3:p.Pro136=
ENST00000394975.2:c.314T>G	ENSP00000378426.2:p.Leu105Arg
ENST00000420057.2:c.276T>G
ENST00000472468.1:c.-2T>G	ENSP00000458994.1:n.-2T>G
ENST00000498155.1:c.411T>G	ENSP00000417662.1:p.Pro137=
ENST00000529564.1:c.283+2000T>G	ENSP00000431371.1:n.283+2000T>G
ENST00000532364.1:c.173+3245T>G	ENSP00000460316.1:n.173+3245T>G
ENST00000533518.5:c.187T>G
NM_001311311.1:c.398T>G	NP_001298240.1:p.Leu133Arg
NM_024006.4:c.314T>G	NP_076869.1:p.Leu105Arg
NM_024006.5:c.314T>G	NP_076869.1:p.Leu105Arg
NM_206824.1:c.204T>G	NP_996560.1:p.Pro68=
NM_206824.2:c.204T>G	NP_996560.1:p.Pro68=
XM_011545944.1:c.314T>G	XP_011544246.1:p.Leu105Arg
XM_011545945.1:c.204T>G	XP_011544247.1:p.Pro68=
XR_950848.1:n.1102T>G
NM_024006.6:c.314T>G MANE Select	NP_076869.1:p.Leu105Arg
NM_001311311.2:c.398T>G	NP_001298240.1:p.Leu133Arg
NM_206824.3:c.204T>G	NP_996560.1:p.Pro68=