Canonical Allele Identifier: CA2632821318

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31090977-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090977C>A , CM000678.2:g.31090977C>A	GRCh38
NC_000016.9:g.31102298C>A , CM000678.1:g.31102298C>A	GRCh37
NC_000016.8:g.31009799C>A	NCBI36
NG_011564.1:g.8979G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*157G>T MANE Select	ENSP00000378426.2:n.*157G>T
ENST00000300851.10:c.*260G>T	ENSP00000300851.6:n.*260G>T
ENST00000319788.11:c.*260G>T	ENSP00000326135.7:n.*260G>T
ENST00000354895.4:c.*260G>T	ENSP00000346969.4:n.*260G>T
ENST00000394975.2:c.*157G>T	ENSP00000378426.2:n.*157G>T
ENST00000420057.2:c.611G>T
ENST00000529564.1:c.283+2335G>T	ENSP00000431371.1:n.283+2335G>T
ENST00000532364.1:c.173+3580G>T	ENSP00000460316.1:n.173+3580G>T
ENST00000533518.5:c.407+115G>T
NM_001311311.1:c.*157G>T	NP_001298240.1:n.*157G>T
NM_024006.4:c.*157G>T	NP_076869.1:n.*157G>T
NM_024006.5:c.*157G>T	NP_076869.1:n.*157G>T
NM_206824.1:c.*260G>T	NP_996560.1:n.*260G>T
NM_206824.2:c.*260G>T	NP_996560.1:n.*260G>T
XM_011545944.1:c.*157G>T	XP_011544246.1:n.*157G>T
XM_011545945.1:c.*260G>T	XP_011544247.1:n.*260G>T
XR_950848.1:n.1437G>T
NM_024006.6:c.*157G>T MANE Select	NP_076869.1:n.*157G>T
NM_001311311.2:c.*157G>T	NP_001298240.1:n.*157G>T
NM_206824.3:c.*260G>T	NP_996560.1:n.*260G>T