Canonical Allele Identifier: CA2216888738
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091006T= , CM000678.2:g.31091006T= GRCh38
NC_000016.9:g.31102327T= , CM000678.1:g.31102327T= GRCh37
NC_000016.8:g.31009828T= NCBI36
NG_011564.1:g.8950A=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*128A= MANE Select ENSP00000378426.2:n.*128A=
ENST00000300851.10:c.*231A= ENSP00000300851.6:n.*231A=
ENST00000319788.11:c.*231A= ENSP00000326135.7:n.*231A=
ENST00000354895.4:c.*231A= ENSP00000346969.4:n.*231A=
ENST00000394975.2:c.*128A= ENSP00000378426.2:n.*128A=
ENST00000420057.2:c.582A=
ENST00000529564.1:c.283+2306A= ENSP00000431371.1:n.283+2306A=
ENST00000532364.1:c.173+3551A= ENSP00000460316.1:n.173+3551A=
ENST00000533518.5:c.407+86A=
NM_001311311.1:c.*128A= NP_001298240.1:n.*128A=
NM_024006.4:c.*128A= NP_076869.1:n.*128A=
NM_024006.5:c.*128A= NP_076869.1:n.*128A=
NM_206824.1:c.*231A= NP_996560.1:n.*231A=
NM_206824.2:c.*231A= NP_996560.1:n.*231A=
XM_011545944.1:c.*128A= XP_011544246.1:n.*128A=
XM_011545945.1:c.*231A= XP_011544247.1:n.*231A=
XR_950848.1:n.1408A=
NM_024006.6:c.*128A= MANE Select NP_076869.1:n.*128A=
NM_001311311.2:c.*128A= NP_001298240.1:n.*128A=
NM_206824.3:c.*231A= NP_996560.1:n.*231A=