Canonical Allele Identifier: CA976332678

Gene: VKORC1

Linked Data

• dbSNP Id: rs2057285016
• gnomAD v3: 16-31091022-TA-T
• gnomAD v4: 16-31091022-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091024del , CM000678.2:g.31091024del	GRCh38
NC_000016.9:g.31102345del , CM000678.1:g.31102345del	GRCh37
NC_000016.8:g.31009846del	NCBI36
NG_011564.1:g.8933del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*111del MANE Select	ENSP00000378426.2:n.*111del
ENST00000300851.10:c.*214del	ENSP00000300851.6:n.*214del
ENST00000319788.11:c.*214del	ENSP00000326135.7:n.*214del
ENST00000354895.4:c.*214del	ENSP00000346969.4:n.*214del
ENST00000394975.2:c.*111del	ENSP00000378426.2:n.*111del
ENST00000420057.2:c.565del
ENST00000529564.1:c.283+2289del	ENSP00000431371.1:n.283+2289del
ENST00000532364.1:c.173+3534del	ENSP00000460316.1:n.173+3534del
ENST00000533518.5:c.407+69del
NM_001311311.1:c.*111del	NP_001298240.1:n.*111del
NM_024006.4:c.*111del	NP_076869.1:n.*111del
NM_024006.5:c.*111del	NP_076869.1:n.*111del
NM_206824.1:c.*214del	NP_996560.1:n.*214del
NM_206824.2:c.*214del	NP_996560.1:n.*214del
XM_011545944.1:c.*111del	XP_011544246.1:n.*111del
XM_011545945.1:c.*214del	XP_011544247.1:n.*214del
XR_950848.1:n.1391del
NM_024006.6:c.*111del MANE Select	NP_076869.1:n.*111del
NM_001311311.2:c.*111del	NP_001298240.1:n.*111del
NM_206824.3:c.*214del	NP_996560.1:n.*214del