Canonical Allele Identifier: CA2632821310

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31090974-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090976del , CM000678.2:g.31090976del	GRCh38
NC_000016.9:g.31102297del , CM000678.1:g.31102297del	GRCh37
NC_000016.8:g.31009798del	NCBI36
NG_011564.1:g.8981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*159del MANE Select	ENSP00000378426.2:n.*159del
ENST00000300851.10:c.*262del	ENSP00000300851.6:n.*262del
ENST00000319788.11:c.*262del	ENSP00000326135.7:n.*262del
ENST00000354895.4:c.*262del	ENSP00000346969.4:n.*262del
ENST00000394975.2:c.*159del	ENSP00000378426.2:n.*159del
ENST00000420057.2:c.613del
ENST00000529564.1:c.283+2337del	ENSP00000431371.1:n.283+2337del
ENST00000532364.1:c.173+3582del	ENSP00000460316.1:n.173+3582del
ENST00000533518.5:c.407+117del
NM_001311311.1:c.*159del	NP_001298240.1:n.*159del
NM_024006.4:c.*159del	NP_076869.1:n.*159del
NM_024006.5:c.*159del	NP_076869.1:n.*159del
NM_206824.1:c.*262del	NP_996560.1:n.*262del
NM_206824.2:c.*262del	NP_996560.1:n.*262del
XM_011545944.1:c.*159del	XP_011544246.1:n.*159del
XM_011545945.1:c.*262del	XP_011544247.1:n.*262del
XR_950848.1:n.1439del
NM_024006.6:c.*159del MANE Select	NP_076869.1:n.*159del
NM_001311311.2:c.*159del	NP_001298240.1:n.*159del
NM_206824.3:c.*262del	NP_996560.1:n.*262del