Canonical Allele Identifier: CA2806495354
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093705_31093706insG , CM000678.2:g.31093705_31093706insG GRCh38
NC_000016.9:g.31105026_31105027insG , CM000678.1:g.31105026_31105027insG GRCh37
NC_000016.8:g.31012527_31012528insG NCBI36
NG_011564.1:g.6250_6251insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-285_174-284insC MANE Select ENSP00000378426.2:n.174-285_174-284insC
ENST00000300851.10:c.174-224_174-223insC ENSP00000300851.6:n.174-224_174-223insC
ENST00000319788.11:c.174-285_174-284insC ENSP00000326135.7:n.174-285_174-284insC
ENST00000354895.4:c.173+851_173+852insC ENSP00000346969.4:n.173+851_173+852insC
ENST00000394971.7:c.268-285_268-284insC ENSP00000378422.3:n.268-285_268-284insC
ENST00000394975.2:c.174-285_174-284insC ENSP00000378426.2:n.174-285_174-284insC
ENST00000420057.2:c.245+1683_245+1684insC
ENST00000498155.1:c.271-285_271-284insC ENSP00000417662.1:n.271-285_271-284insC
ENST00000529564.1:c.174-285_174-284insC ENSP00000431371.1:n.174-285_174-284insC
ENST00000532364.1:c.173+851_173+852insC ENSP00000460316.1:n.173+851_173+852insC
ENST00000533518.5:c.47-285_47-284insC
NM_001311311.1:c.174-285_174-284insC NP_001298240.1:n.174-285_174-284insC
NM_024006.4:c.174-285_174-284insC NP_076869.1:n.174-285_174-284insC
NM_024006.5:c.174-285_174-284insC NP_076869.1:n.174-285_174-284insC
NM_206824.1:c.173+851_173+852insC NP_996560.1:n.173+851_173+852insC
NM_206824.2:c.173+851_173+852insC NP_996560.1:n.173+851_173+852insC
XM_011545944.1:c.174-285_174-284insC XP_011544246.1:n.174-285_174-284insC
XM_011545945.1:c.173+851_173+852insC XP_011544247.1:n.173+851_173+852insC
XR_950848.1:n.962-285_962-284insC
NM_024006.6:c.174-285_174-284insC MANE Select NP_076869.1:n.174-285_174-284insC
NM_001311311.2:c.174-285_174-284insC NP_001298240.1:n.174-285_174-284insC
NM_206824.3:c.173+851_173+852insC NP_996560.1:n.173+851_173+852insC