Canonical Allele Identifier: CA976334295
Gene: VKORC1 HGNC NCBI

Linked Data

dbSNP Id: rs1567421749

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093698_31093699insTT , CM000678.2:g.31093698_31093699insTT GRCh38
NC_000016.9:g.31105019_31105020insTT , CM000678.1:g.31105019_31105020insTT GRCh37
NC_000016.8:g.31012520_31012521insTT NCBI36
NG_011564.1:g.6258_6259insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-277_174-276insAA MANE Select ENSP00000378426.2:n.174-277_174-276insAA
ENST00000300851.10:c.174-216_174-215insAA ENSP00000300851.6:n.174-216_174-215insAA
ENST00000319788.11:c.174-277_174-276insAA ENSP00000326135.7:n.174-277_174-276insAA
ENST00000354895.4:c.173+859_173+860insAA ENSP00000346969.4:n.173+859_173+860insAA
ENST00000394971.7:c.268-277_268-276insAA ENSP00000378422.3:n.268-277_268-276insAA
ENST00000394975.2:c.174-277_174-276insAA ENSP00000378426.2:n.174-277_174-276insAA
ENST00000420057.2:c.245+1691_245+1692insAA
ENST00000498155.1:c.271-277_271-276insAA ENSP00000417662.1:n.271-277_271-276insAA
ENST00000529564.1:c.174-277_174-276insAA ENSP00000431371.1:n.174-277_174-276insAA
ENST00000532364.1:c.173+859_173+860insAA ENSP00000460316.1:n.173+859_173+860insAA
ENST00000533518.5:c.47-277_47-276insAA
NM_001311311.1:c.174-277_174-276insAA NP_001298240.1:n.174-277_174-276insAA
NM_024006.4:c.174-277_174-276insAA NP_076869.1:n.174-277_174-276insAA
NM_024006.5:c.174-277_174-276insAA NP_076869.1:n.174-277_174-276insAA
NM_206824.1:c.173+859_173+860insAA NP_996560.1:n.173+859_173+860insAA
NM_206824.2:c.173+859_173+860insAA NP_996560.1:n.173+859_173+860insAA
XM_011545944.1:c.174-277_174-276insAA XP_011544246.1:n.174-277_174-276insAA
XM_011545945.1:c.173+859_173+860insAA XP_011544247.1:n.173+859_173+860insAA
XR_950848.1:n.962-277_962-276insAA
NM_024006.6:c.174-277_174-276insAA MANE Select NP_076869.1:n.174-277_174-276insAA
NM_001311311.2:c.174-277_174-276insAA NP_001298240.1:n.174-277_174-276insAA
NM_206824.3:c.173+859_173+860insAA NP_996560.1:n.173+859_173+860insAA