Canonical Allele Identifier: CA8021229

Gene: VKORC1

Linked Data

• dbSNP Id: rs774801918
• ExAC: 16:31105544 A / AC
• gnomAD v2: 16-31105544-A-AC
• gnomAD v3: 16-31094223-A-AC
• gnomAD v4: 16-31094223-A-AC
• MyVariant Identifiers: chr16:g.31105545_31105546insC (hg19) ; chr16:g.31105544_31105545insC (hg19) ; chr16:g.31094223_31094224insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094229dup , CM000678.2:g.31094229dup	GRCh38
NC_000016.9:g.31105550dup , CM000678.1:g.31105550dup	GRCh37
NC_000016.8:g.31013051dup	NCBI36
NG_011564.1:g.5732dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.173+333dup MANE Select	ENSP00000378426.2:n.173+333dup
ENST00000300851.10:c.173+333dup	ENSP00000300851.6:n.173+333dup
ENST00000319788.11:c.173+333dup	ENSP00000326135.7:n.173+333dup
ENST00000354895.4:c.173+333dup	ENSP00000346969.4:n.173+333dup
ENST00000394971.7:c.267+11dup	ENSP00000378422.3:n.267+11dup
ENST00000394975.2:c.173+333dup	ENSP00000378426.2:n.173+333dup
ENST00000420057.2:c.245+1165dup
ENST00000498155.1:c.271-803dup	ENSP00000417662.1:n.271-803dup
ENST00000529564.1:c.173+333dup	ENSP00000431371.1:n.173+333dup
ENST00000532364.1:c.173+333dup	ENSP00000460316.1:n.173+333dup
ENST00000533518.5:c.46+333dup
NM_001311311.1:c.173+333dup	NP_001298240.1:n.173+333dup
NM_024006.4:c.173+333dup	NP_076869.1:n.173+333dup
NM_024006.5:c.173+333dup	NP_076869.1:n.173+333dup
NM_206824.1:c.173+333dup	NP_996560.1:n.173+333dup
NM_206824.2:c.173+333dup	NP_996560.1:n.173+333dup
XM_011545944.1:c.173+333dup	XP_011544246.1:n.173+333dup
XM_011545945.1:c.173+333dup	XP_011544247.1:n.173+333dup
XR_950848.1:n.961+333dup
NM_024006.6:c.173+333dup MANE Select	NP_076869.1:n.173+333dup
NM_001311311.2:c.173+333dup	NP_001298240.1:n.173+333dup
NM_206824.3:c.173+333dup	NP_996560.1:n.173+333dup