Canonical Allele Identifier: CA2216892956
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093882_31093895delinsTTTTTGGTAGAGAC , CM000678.2:g.31093882_31093895delinsTTTTTGGTAGAGAC GRCh38
NC_000016.9:g.31105203_31105216delinsTTTTTGGTAGAGAC , CM000678.1:g.31105203_31105216delinsTTTTTGGTAGAGAC GRCh37
NC_000016.8:g.31012704_31012717delinsTTTTTGGTAGAGAC NCBI36
NG_011564.1:g.6061_6074delinsGTCTCTACCAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-474_174-461delinsGTCTCTACCAAAAA MANE Select ENSP00000378426.2:n.174-474_174-461delinsGTCTCTACCAAAAA
ENST00000300851.10:c.174-413_174-400delinsGTCTCTACCAAAAA ENSP00000300851.6:n.174-413_174-400delinsGTCTCTACCAAAAA
ENST00000319788.11:c.174-474_174-461delinsGTCTCTACCAAAAA ENSP00000326135.7:n.174-474_174-461delinsGTCTCTACCAAAAA
ENST00000354895.4:c.173+662_173+675delinsGTCTCTACCAAAAA ENSP00000346969.4:n.173+662_173+675delinsGTCTCTACCAAAAA
ENST00000394971.7:c.267+340_267+353delinsGTCTCTACCAAAAA ENSP00000378422.3:n.267+340_267+353delinsGTCTCTACCAAAAA
ENST00000394975.2:c.174-474_174-461delinsGTCTCTACCAAAAA ENSP00000378426.2:n.174-474_174-461delinsGTCTCTACCAAAAA
ENST00000420057.2:c.245+1494_245+1507delinsGTCTCTACCAAAAA
ENST00000498155.1:c.271-474_271-461delinsGTCTCTACCAAAAA ENSP00000417662.1:n.271-474_271-461delinsGTCTCTACCAAAAA
ENST00000529564.1:c.174-474_174-461delinsGTCTCTACCAAAAA ENSP00000431371.1:n.174-474_174-461delinsGTCTCTACCAAAAA
ENST00000532364.1:c.173+662_173+675delinsGTCTCTACCAAAAA ENSP00000460316.1:n.173+662_173+675delinsGTCTCTACCAAAAA
ENST00000533518.5:c.47-474_47-461delinsGTCTCTACCAAAAA
NM_001311311.1:c.174-474_174-461delinsGTCTCTACCAAAAA NP_001298240.1:n.174-474_174-461delinsGTCTCTACCAAAAA
NM_024006.4:c.174-474_174-461delinsGTCTCTACCAAAAA NP_076869.1:n.174-474_174-461delinsGTCTCTACCAAAAA
NM_024006.5:c.174-474_174-461delinsGTCTCTACCAAAAA NP_076869.1:n.174-474_174-461delinsGTCTCTACCAAAAA
NM_206824.1:c.173+662_173+675delinsGTCTCTACCAAAAA NP_996560.1:n.173+662_173+675delinsGTCTCTACCAAAAA
NM_206824.2:c.173+662_173+675delinsGTCTCTACCAAAAA NP_996560.1:n.173+662_173+675delinsGTCTCTACCAAAAA
XM_011545944.1:c.174-474_174-461delinsGTCTCTACCAAAAA XP_011544246.1:n.174-474_174-461delinsGTCTCTACCAAAAA
XM_011545945.1:c.173+662_173+675delinsGTCTCTACCAAAAA XP_011544247.1:n.173+662_173+675delinsGTCTCTACCAAAAA
XR_950848.1:n.962-474_962-461delinsGTCTCTACCAAAAA
NM_024006.6:c.174-474_174-461delinsGTCTCTACCAAAAA MANE Select NP_076869.1:n.174-474_174-461delinsGTCTCTACCAAAAA
NM_001311311.2:c.174-474_174-461delinsGTCTCTACCAAAAA NP_001298240.1:n.174-474_174-461delinsGTCTCTACCAAAAA
NM_206824.3:c.173+662_173+675delinsGTCTCTACCAAAAA NP_996560.1:n.173+662_173+675delinsGTCTCTACCAAAAA