Canonical Allele Identifier: CA2843013878

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091056G>T , CM000678.2:g.31091056G>T	GRCh38
NC_000016.9:g.31102377G>T , CM000678.1:g.31102377G>T	GRCh37
NC_000016.8:g.31009878G>T	NCBI36
NG_011564.1:g.8900C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*78C>A MANE Select	ENSP00000378426.2:n.*78C>A
ENST00000300851.10:c.*181C>A	ENSP00000300851.6:n.*181C>A
ENST00000319788.11:c.*181C>A	ENSP00000326135.7:n.*181C>A
ENST00000354895.4:c.*181C>A	ENSP00000346969.4:n.*181C>A
ENST00000394975.2:c.*78C>A	ENSP00000378426.2:n.*78C>A
ENST00000420057.2:c.532C>A
ENST00000529564.1:c.283+2256C>A	ENSP00000431371.1:n.283+2256C>A
ENST00000532364.1:c.173+3501C>A	ENSP00000460316.1:n.173+3501C>A
ENST00000533518.5:c.407+36C>A
NM_001311311.1:c.*78C>A	NP_001298240.1:n.*78C>A
NM_024006.4:c.*78C>A	NP_076869.1:n.*78C>A
NM_024006.5:c.*78C>A	NP_076869.1:n.*78C>A
NM_206824.1:c.*181C>A	NP_996560.1:n.*181C>A
NM_206824.2:c.*181C>A	NP_996560.1:n.*181C>A
XM_011545944.1:c.*78C>A	XP_011544246.1:n.*78C>A
XM_011545945.1:c.*181C>A	XP_011544247.1:n.*181C>A
XR_950848.1:n.1358C>A
NM_024006.6:c.*78C>A MANE Select	NP_076869.1:n.*78C>A
NM_001311311.2:c.*78C>A	NP_001298240.1:n.*78C>A
NM_206824.3:c.*181C>A	NP_996560.1:n.*181C>A