Canonical Allele Identifier: CA395729177
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091157G>T , CM000678.2:g.31091157G>T GRCh38
NC_000016.9:g.31102478G>T , CM000678.1:g.31102478G>T GRCh37
NC_000016.8:g.31009979G>T NCBI36
NG_011564.1:g.8799C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.469C>A MANE Select ENSP00000378426.2:p.Gln157Lys
ENST00000300851.10:c.*80C>A ENSP00000300851.6:n.*80C>A
ENST00000319788.11:c.*80C>A ENSP00000326135.7:n.*80C>A
ENST00000354895.4:c.*80C>A ENSP00000346969.4:n.*80C>A
ENST00000394971.7:c.*80C>A ENSP00000378422.3:n.*80C>A
ENST00000394975.2:c.469C>A ENSP00000378426.2:p.Gln157Lys
ENST00000420057.2:c.431C>A
ENST00000529564.1:c.283+2155C>A ENSP00000431371.1:n.283+2155C>A
ENST00000532364.1:c.173+3400C>A ENSP00000460316.1:n.173+3400C>A
ENST00000533518.5:c.342C>A
NM_001311311.1:c.553C>A NP_001298240.1:p.Gln185Lys
NM_024006.4:c.469C>A NP_076869.1:p.Gln157Lys
NM_024006.5:c.469C>A NP_076869.1:p.Gln157Lys
NM_206824.1:c.*80C>A NP_996560.1:n.*80C>A
NM_206824.2:c.*80C>A NP_996560.1:n.*80C>A
XM_011545944.1:c.469C>A XP_011544246.1:p.Gln157Lys
XM_011545945.1:c.*80C>A XP_011544247.1:n.*80C>A
XR_950848.1:n.1257C>A
NM_024006.6:c.469C>A MANE Select NP_076869.1:p.Gln157Lys
NM_001311311.2:c.553C>A NP_001298240.1:p.Gln185Lys
NM_206824.3:c.*80C>A NP_996560.1:n.*80C>A