Canonical Allele Identifier: CA2632821398

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31091016-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091021del , CM000678.2:g.31091021del	GRCh38
NC_000016.9:g.31102342del , CM000678.1:g.31102342del	GRCh37
NC_000016.8:g.31009843del	NCBI36
NG_011564.1:g.8939del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.*117del MANE Select	ENSP00000378426.2:n.*117del
ENST00000300851.10:c.*220del	ENSP00000300851.6:n.*220del
ENST00000319788.11:c.*220del	ENSP00000326135.7:n.*220del
ENST00000354895.4:c.*220del	ENSP00000346969.4:n.*220del
ENST00000394975.2:c.*117del	ENSP00000378426.2:n.*117del
ENST00000420057.2:c.571del
ENST00000529564.1:c.283+2295del	ENSP00000431371.1:n.283+2295del
ENST00000532364.1:c.173+3540del	ENSP00000460316.1:n.173+3540del
ENST00000533518.5:c.407+75del
NM_001311311.1:c.*117del	NP_001298240.1:n.*117del
NM_024006.4:c.*117del	NP_076869.1:n.*117del
NM_024006.5:c.*117del	NP_076869.1:n.*117del
NM_206824.1:c.*220del	NP_996560.1:n.*220del
NM_206824.2:c.*220del	NP_996560.1:n.*220del
XM_011545944.1:c.*117del	XP_011544246.1:n.*117del
XM_011545945.1:c.*220del	XP_011544247.1:n.*220del
XR_950848.1:n.1397del
NM_024006.6:c.*117del MANE Select	NP_076869.1:n.*117del
NM_001311311.2:c.*117del	NP_001298240.1:n.*117del
NM_206824.3:c.*220del	NP_996560.1:n.*220del