Canonical Allele Identifier: CA621876753
Gene: VKORC1 HGNC NCBI

Linked Data

dbSNP Id: rs1491508372

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093700_31093701insC , CM000678.2:g.31093700_31093701insC GRCh38
NC_000016.9:g.31105021_31105022insC , CM000678.1:g.31105021_31105022insC GRCh37
NC_000016.8:g.31012522_31012523insC NCBI36
NG_011564.1:g.6255_6256insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-280_174-279insG MANE Select ENSP00000378426.2:n.174-280_174-279insG
ENST00000300851.10:c.174-219_174-218insG ENSP00000300851.6:n.174-219_174-218insG
ENST00000319788.11:c.174-280_174-279insG ENSP00000326135.7:n.174-280_174-279insG
ENST00000354895.4:c.173+856_173+857insG ENSP00000346969.4:n.173+856_173+857insG
ENST00000394971.7:c.268-280_268-279insG ENSP00000378422.3:n.268-280_268-279insG
ENST00000394975.2:c.174-280_174-279insG ENSP00000378426.2:n.174-280_174-279insG
ENST00000420057.2:c.245+1688_245+1689insG
ENST00000498155.1:c.271-280_271-279insG ENSP00000417662.1:n.271-280_271-279insG
ENST00000529564.1:c.174-280_174-279insG ENSP00000431371.1:n.174-280_174-279insG
ENST00000532364.1:c.173+856_173+857insG ENSP00000460316.1:n.173+856_173+857insG
ENST00000533518.5:c.47-280_47-279insG
NM_001311311.1:c.174-280_174-279insG NP_001298240.1:n.174-280_174-279insG
NM_024006.4:c.174-280_174-279insG NP_076869.1:n.174-280_174-279insG
NM_024006.5:c.174-280_174-279insG NP_076869.1:n.174-280_174-279insG
NM_206824.1:c.173+856_173+857insG NP_996560.1:n.173+856_173+857insG
NM_206824.2:c.173+856_173+857insG NP_996560.1:n.173+856_173+857insG
XM_011545944.1:c.174-280_174-279insG XP_011544246.1:n.174-280_174-279insG
XM_011545945.1:c.173+856_173+857insG XP_011544247.1:n.173+856_173+857insG
XR_950848.1:n.962-280_962-279insG
NM_024006.6:c.174-280_174-279insG MANE Select NP_076869.1:n.174-280_174-279insG
NM_001311311.2:c.174-280_174-279insG NP_001298240.1:n.174-280_174-279insG
NM_206824.3:c.173+856_173+857insG NP_996560.1:n.173+856_173+857insG