Canonical Allele Identifier: CA2216892341
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093699_31093716delinsCTTTTTTTTTTTTTTTTT , CM000678.2:g.31093699_31093716delinsCTTTTTTTTTTTTTTTTT GRCh38
NC_000016.9:g.31105020_31105037delinsCTTTTTTTTTTTTTTTTT , CM000678.1:g.31105020_31105037delinsCTTTTTTTTTTTTTTTTT GRCh37
NC_000016.8:g.31012521_31012538delinsCTTTTTTTTTTTTTTTTT NCBI36
NG_011564.1:g.6240_6257delinsAAAAAAAAAAAAAAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG MANE Select ENSP00000378426.2:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
ENST00000300851.10:c.174-234_174-217delinsAAAAAAAAAAAAAAAAAG ENSP00000300851.6:n.174-234_174-217delinsAAAAAAAAAAAAAAAAAG
ENST00000319788.11:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG ENSP00000326135.7:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
ENST00000354895.4:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG ENSP00000346969.4:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG
ENST00000394971.7:c.268-295_268-278delinsAAAAAAAAAAAAAAAAAG ENSP00000378422.3:n.268-295_268-278delinsAAAAAAAAAAAAAAAAAG
ENST00000394975.2:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG ENSP00000378426.2:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
ENST00000420057.2:c.245+1673_245+1690delinsAAAAAAAAAAAAAAAAAG
ENST00000498155.1:c.271-295_271-278delinsAAAAAAAAAAAAAAAAAG ENSP00000417662.1:n.271-295_271-278delinsAAAAAAAAAAAAAAAAAG
ENST00000529564.1:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG ENSP00000431371.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
ENST00000532364.1:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG ENSP00000460316.1:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG
ENST00000533518.5:c.47-295_47-278delinsAAAAAAAAAAAAAAAAAG
NM_001311311.1:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG NP_001298240.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
NM_024006.4:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG NP_076869.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
NM_024006.5:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG NP_076869.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
NM_206824.1:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG NP_996560.1:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG
NM_206824.2:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG NP_996560.1:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG
XM_011545944.1:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG XP_011544246.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
XM_011545945.1:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG XP_011544247.1:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG
XR_950848.1:n.962-295_962-278delinsAAAAAAAAAAAAAAAAAG
NM_024006.6:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG MANE Select NP_076869.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
NM_001311311.2:c.174-295_174-278delinsAAAAAAAAAAAAAAAAAG NP_001298240.1:n.174-295_174-278delinsAAAAAAAAAAAAAAAAAG
NM_206824.3:c.173+841_173+858delinsAAAAAAAAAAAAAAAAAG NP_996560.1:n.173+841_173+858delinsAAAAAAAAAAAAAAAAAG