Canonical Allele Identifier: CA395729176

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102478G>C (hg19) ; chr16:g.31091157G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091157G>C , CM000678.2:g.31091157G>C	GRCh38
NC_000016.9:g.31102478G>C , CM000678.1:g.31102478G>C	GRCh37
NC_000016.8:g.31009979G>C	NCBI36
NG_011564.1:g.8799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.469C>G MANE Select	ENSP00000378426.2:p.Gln157Glu
ENST00000300851.10:c.*80C>G	ENSP00000300851.6:n.*80C>G
ENST00000319788.11:c.*80C>G	ENSP00000326135.7:n.*80C>G
ENST00000354895.4:c.*80C>G	ENSP00000346969.4:n.*80C>G
ENST00000394971.7:c.*80C>G	ENSP00000378422.3:n.*80C>G
ENST00000394975.2:c.469C>G	ENSP00000378426.2:p.Gln157Glu
ENST00000420057.2:c.431C>G
ENST00000529564.1:c.283+2155C>G	ENSP00000431371.1:n.283+2155C>G
ENST00000532364.1:c.173+3400C>G	ENSP00000460316.1:n.173+3400C>G
ENST00000533518.5:c.342C>G
NM_001311311.1:c.553C>G	NP_001298240.1:p.Gln185Glu
NM_024006.4:c.469C>G	NP_076869.1:p.Gln157Glu
NM_024006.5:c.469C>G	NP_076869.1:p.Gln157Glu
NM_206824.1:c.*80C>G	NP_996560.1:n.*80C>G
NM_206824.2:c.*80C>G	NP_996560.1:n.*80C>G
XM_011545944.1:c.469C>G	XP_011544246.1:p.Gln157Glu
XM_011545945.1:c.*80C>G	XP_011544247.1:n.*80C>G
XR_950848.1:n.1257C>G
NM_024006.6:c.469C>G MANE Select	NP_076869.1:p.Gln157Glu
NM_001311311.2:c.553C>G	NP_001298240.1:p.Gln185Glu
NM_206824.3:c.*80C>G	NP_996560.1:n.*80C>G