Canonical Allele Identifier: CA2632821379

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31091005-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091005A>C , CM000678.2:g.31091005A>C	GRCh38
NC_000016.9:g.31102326A>C , CM000678.1:g.31102326A>C	GRCh37
NC_000016.8:g.31009827A>C	NCBI36
NG_011564.1:g.8951T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*129T>G MANE Select	ENSP00000378426.2:n.*129T>G
ENST00000300851.10:c.*232T>G	ENSP00000300851.6:n.*232T>G
ENST00000319788.11:c.*232T>G	ENSP00000326135.7:n.*232T>G
ENST00000354895.4:c.*232T>G	ENSP00000346969.4:n.*232T>G
ENST00000394975.2:c.*129T>G	ENSP00000378426.2:n.*129T>G
ENST00000420057.2:c.583T>G
ENST00000529564.1:c.283+2307T>G	ENSP00000431371.1:n.283+2307T>G
ENST00000532364.1:c.173+3552T>G	ENSP00000460316.1:n.173+3552T>G
ENST00000533518.5:c.407+87T>G
NM_001311311.1:c.*129T>G	NP_001298240.1:n.*129T>G
NM_024006.4:c.*129T>G	NP_076869.1:n.*129T>G
NM_024006.5:c.*129T>G	NP_076869.1:n.*129T>G
NM_206824.1:c.*232T>G	NP_996560.1:n.*232T>G
NM_206824.2:c.*232T>G	NP_996560.1:n.*232T>G
XM_011545944.1:c.*129T>G	XP_011544246.1:n.*129T>G
XM_011545945.1:c.*232T>G	XP_011544247.1:n.*232T>G
XR_950848.1:n.1409T>G
NM_024006.6:c.*129T>G MANE Select	NP_076869.1:n.*129T>G
NM_001311311.2:c.*129T>G	NP_001298240.1:n.*129T>G
NM_206824.3:c.*232T>G	NP_996560.1:n.*232T>G