Canonical Allele Identifier: CA2806498212

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090910A>G , CM000678.2:g.31090910A>G	GRCh38
NC_000016.9:g.31102231A>G , CM000678.1:g.31102231A>G	GRCh37
NC_000016.8:g.31009732A>G	NCBI36
NG_011564.1:g.9046T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*224T>C MANE Select	ENSP00000378426.2:n.*224T>C
ENST00000300851.10:c.*327T>C	ENSP00000300851.6:n.*327T>C
ENST00000319788.11:c.*327T>C	ENSP00000326135.7:n.*327T>C
ENST00000354895.4:c.*327T>C	ENSP00000346969.4:n.*327T>C
ENST00000394975.2:c.*224T>C	ENSP00000378426.2:n.*224T>C
ENST00000420057.2:c.678T>C
ENST00000529564.1:c.283+2402T>C	ENSP00000431371.1:n.283+2402T>C
ENST00000532364.1:c.173+3647T>C	ENSP00000460316.1:n.173+3647T>C
ENST00000533518.5:c.407+182T>C
NM_001311311.1:c.*224T>C	NP_001298240.1:n.*224T>C
NM_024006.4:c.*224T>C	NP_076869.1:n.*224T>C
NM_024006.5:c.*224T>C	NP_076869.1:n.*224T>C
NM_206824.1:c.*327T>C	NP_996560.1:n.*327T>C
NM_206824.2:c.*327T>C	NP_996560.1:n.*327T>C
XM_011545944.1:c.*224T>C	XP_011544246.1:n.*224T>C
XM_011545945.1:c.*327T>C	XP_011544247.1:n.*327T>C
XR_950848.1:n.1504T>C
NM_024006.6:c.*224T>C MANE Select	NP_076869.1:n.*224T>C
NM_001311311.2:c.*224T>C	NP_001298240.1:n.*224T>C
NM_206824.3:c.*327T>C	NP_996560.1:n.*327T>C