Canonical Allele Identifier: CA2632821332

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31090987-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090987C>T , CM000678.2:g.31090987C>T	GRCh38
NC_000016.9:g.31102308C>T , CM000678.1:g.31102308C>T	GRCh37
NC_000016.8:g.31009809C>T	NCBI36
NG_011564.1:g.8969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*147G>A MANE Select	ENSP00000378426.2:n.*147G>A
ENST00000300851.10:c.*250G>A	ENSP00000300851.6:n.*250G>A
ENST00000319788.11:c.*250G>A	ENSP00000326135.7:n.*250G>A
ENST00000354895.4:c.*250G>A	ENSP00000346969.4:n.*250G>A
ENST00000394975.2:c.*147G>A	ENSP00000378426.2:n.*147G>A
ENST00000420057.2:c.601G>A
ENST00000529564.1:c.283+2325G>A	ENSP00000431371.1:n.283+2325G>A
ENST00000532364.1:c.173+3570G>A	ENSP00000460316.1:n.173+3570G>A
ENST00000533518.5:c.407+105G>A
NM_001311311.1:c.*147G>A	NP_001298240.1:n.*147G>A
NM_024006.4:c.*147G>A	NP_076869.1:n.*147G>A
NM_024006.5:c.*147G>A	NP_076869.1:n.*147G>A
NM_206824.1:c.*250G>A	NP_996560.1:n.*250G>A
NM_206824.2:c.*250G>A	NP_996560.1:n.*250G>A
XM_011545944.1:c.*147G>A	XP_011544246.1:n.*147G>A
XM_011545945.1:c.*250G>A	XP_011544247.1:n.*250G>A
XR_950848.1:n.1427G>A
NM_024006.6:c.*147G>A MANE Select	NP_076869.1:n.*147G>A
NM_001311311.2:c.*147G>A	NP_001298240.1:n.*147G>A
NM_206824.3:c.*250G>A	NP_996560.1:n.*250G>A