Canonical Allele Identifier: CA2216888593
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31090950_31090951delinsTG , CM000678.2:g.31090950_31090951delinsTG GRCh38
NC_000016.9:g.31102271_31102272delinsTG , CM000678.1:g.31102271_31102272delinsTG GRCh37
NC_000016.8:g.31009772_31009773delinsTG NCBI36
NG_011564.1:g.9005_9006delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.*183_*184delinsCA MANE Select ENSP00000378426.2:n.*183_*184delinsCA
ENST00000300851.10:c.*286_*287delinsCA ENSP00000300851.6:n.*286_*287delinsCA
ENST00000319788.11:c.*286_*287delinsCA ENSP00000326135.7:n.*286_*287delinsCA
ENST00000354895.4:c.*286_*287delinsCA ENSP00000346969.4:n.*286_*287delinsCA
ENST00000394975.2:c.*183_*184delinsCA ENSP00000378426.2:n.*183_*184delinsCA
ENST00000420057.2:c.637_638delinsCA
ENST00000529564.1:c.283+2361_283+2362delinsCA ENSP00000431371.1:n.283+2361_283+2362delinsCA
ENST00000532364.1:c.173+3606_173+3607delinsCA ENSP00000460316.1:n.173+3606_173+3607delinsCA
ENST00000533518.5:c.407+141_407+142delinsCA
NM_001311311.1:c.*183_*184delinsCA NP_001298240.1:n.*183_*184delinsCA
NM_024006.4:c.*183_*184delinsCA NP_076869.1:n.*183_*184delinsCA
NM_024006.5:c.*183_*184delinsCA NP_076869.1:n.*183_*184delinsCA
NM_206824.1:c.*286_*287delinsCA NP_996560.1:n.*286_*287delinsCA
NM_206824.2:c.*286_*287delinsCA NP_996560.1:n.*286_*287delinsCA
XM_011545944.1:c.*183_*184delinsCA XP_011544246.1:n.*183_*184delinsCA
XM_011545945.1:c.*286_*287delinsCA XP_011544247.1:n.*286_*287delinsCA
XR_950848.1:n.1463_1464delinsCA
NM_024006.6:c.*183_*184delinsCA MANE Select NP_076869.1:n.*183_*184delinsCA
NM_001311311.2:c.*183_*184delinsCA NP_001298240.1:n.*183_*184delinsCA
NM_206824.3:c.*286_*287delinsCA NP_996560.1:n.*286_*287delinsCA