Canonical Allele Identifier: CA2632821373

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31091003-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091004del , CM000678.2:g.31091004del	GRCh38
NC_000016.9:g.31102325del , CM000678.1:g.31102325del	GRCh37
NC_000016.8:g.31009826del	NCBI36
NG_011564.1:g.8952del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.*130del MANE Select	ENSP00000378426.2:n.*130del
ENST00000300851.10:c.*233del	ENSP00000300851.6:n.*233del
ENST00000319788.11:c.*233del	ENSP00000326135.7:n.*233del
ENST00000354895.4:c.*233del	ENSP00000346969.4:n.*233del
ENST00000394975.2:c.*130del	ENSP00000378426.2:n.*130del
ENST00000420057.2:c.584del
ENST00000529564.1:c.283+2308del	ENSP00000431371.1:n.283+2308del
ENST00000532364.1:c.173+3553del	ENSP00000460316.1:n.173+3553del
ENST00000533518.5:c.407+88del
NM_001311311.1:c.*130del	NP_001298240.1:n.*130del
NM_024006.4:c.*130del	NP_076869.1:n.*130del
NM_024006.5:c.*130del	NP_076869.1:n.*130del
NM_206824.1:c.*233del	NP_996560.1:n.*233del
NM_206824.2:c.*233del	NP_996560.1:n.*233del
XM_011545944.1:c.*130del	XP_011544246.1:n.*130del
XM_011545945.1:c.*233del	XP_011544247.1:n.*233del
XR_950848.1:n.1410del
NM_024006.6:c.*130del MANE Select	NP_076869.1:n.*130del
NM_001311311.2:c.*130del	NP_001298240.1:n.*130del
NM_206824.3:c.*233del	NP_996560.1:n.*233del