Canonical Allele Identifier: CA2632821177

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31090856-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090856A>G , CM000678.2:g.31090856A>G	GRCh38
NC_000016.9:g.31102177A>G , CM000678.1:g.31102177A>G	GRCh37
NC_000016.8:g.31009678A>G	NCBI36
NG_011564.1:g.9100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*278T>C MANE Select	ENSP00000378426.2:n.*278T>C
ENST00000300851.10:c.*381T>C	ENSP00000300851.6:n.*381T>C
ENST00000319788.11:c.*381T>C	ENSP00000326135.7:n.*381T>C
ENST00000354895.4:c.*381T>C	ENSP00000346969.4:n.*381T>C
ENST00000394975.2:c.*278T>C	ENSP00000378426.2:n.*278T>C
ENST00000420057.2:c.732T>C
ENST00000529564.1:c.283+2456T>C	ENSP00000431371.1:n.283+2456T>C
ENST00000532364.1:c.173+3701T>C	ENSP00000460316.1:n.173+3701T>C
ENST00000533518.5:c.407+236T>C
NM_001311311.1:c.*278T>C	NP_001298240.1:n.*278T>C
NM_024006.4:c.*278T>C	NP_076869.1:n.*278T>C
NM_024006.5:c.*278T>C	NP_076869.1:n.*278T>C
NM_206824.1:c.*381T>C	NP_996560.1:n.*381T>C
NM_206824.2:c.*381T>C	NP_996560.1:n.*381T>C
XM_011545944.1:c.*278T>C	XP_011544246.1:n.*278T>C
XM_011545945.1:c.*381T>C	XP_011544247.1:n.*381T>C
XR_950848.1:n.1558T>C
NM_024006.6:c.*278T>C MANE Select	NP_076869.1:n.*278T>C
NM_001311311.2:c.*278T>C	NP_001298240.1:n.*278T>C
NM_206824.3:c.*381T>C	NP_996560.1:n.*381T>C