Canonical Allele Identifier: CA8021240

Gene: VKORC1

Linked Data

• dbSNP Id: rs760251609
• ExAC: 16:31105608 CGCCT / C
• gnomAD v2: 16-31105608-CGCCT-C
• gnomAD v4: 16-31094287-CGCCT-C
• MyVariant Identifiers: chr16:g.31105609_31105612del (hg19) ; chr16:g.31094288_31094291del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094288_31094291del , CM000678.2:g.31094288_31094291del	GRCh38
NC_000016.9:g.31105609_31105612del , CM000678.1:g.31105609_31105612del	GRCh37
NC_000016.8:g.31013110_31013113del	NCBI36
NG_011564.1:g.5665_5668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.173+266_173+269del MANE Select	ENSP00000378426.2:n.173+266_173+269del
ENST00000300851.10:c.173+266_173+269del	ENSP00000300851.6:n.173+266_173+269del
ENST00000319788.11:c.173+266_173+269del	ENSP00000326135.7:n.173+266_173+269del
ENST00000354895.4:c.173+266_173+269del	ENSP00000346969.4:n.173+266_173+269del
ENST00000394971.7:c.211_214del	ENSP00000378422.3:p.Arg71GlyfsTer7
ENST00000394975.2:c.173+266_173+269del	ENSP00000378426.2:n.173+266_173+269del
ENST00000420057.2:c.245+1098_245+1101del
ENST00000498155.1:c.271-870_271-867del	ENSP00000417662.1:n.271-870_271-867del
ENST00000529564.1:c.173+266_173+269del	ENSP00000431371.1:n.173+266_173+269del
ENST00000532364.1:c.173+266_173+269del	ENSP00000460316.1:n.173+266_173+269del
ENST00000533518.5:c.46+266_46+269del
NM_001311311.1:c.173+266_173+269del	NP_001298240.1:n.173+266_173+269del
NM_024006.4:c.173+266_173+269del	NP_076869.1:n.173+266_173+269del
NM_024006.5:c.173+266_173+269del	NP_076869.1:n.173+266_173+269del
NM_206824.1:c.173+266_173+269del	NP_996560.1:n.173+266_173+269del
NM_206824.2:c.173+266_173+269del	NP_996560.1:n.173+266_173+269del
XM_011545944.1:c.173+266_173+269del	XP_011544246.1:n.173+266_173+269del
XM_011545945.1:c.173+266_173+269del	XP_011544247.1:n.173+266_173+269del
XR_950848.1:n.961+266_961+269del
NM_024006.6:c.173+266_173+269del MANE Select	NP_076869.1:n.173+266_173+269del
NM_001311311.2:c.173+266_173+269del	NP_001298240.1:n.173+266_173+269del
NM_206824.3:c.173+266_173+269del	NP_996560.1:n.173+266_173+269del