Canonical Allele Identifier: CA395729775
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091271A>G , CM000678.2:g.31091271A>G GRCh38
NC_000016.9:g.31102592A>G , CM000678.1:g.31102592A>G GRCh37
NC_000016.8:g.31010093A>G NCBI36
NG_011564.1:g.8685T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.355T>C MANE Select ENSP00000378426.2:p.Tyr119His
ENST00000300851.10:c.416T>C ENSP00000300851.6:p.Leu139Pro
ENST00000319788.11:c.437T>C ENSP00000326135.7:p.Leu146Pro
ENST00000354895.4:c.245T>C ENSP00000346969.4:p.Leu82Pro
ENST00000394971.7:c.449T>C ENSP00000378422.3:p.Leu150Pro
ENST00000394975.2:c.355T>C ENSP00000378426.2:p.Tyr119His
ENST00000420057.2:c.317T>C
ENST00000472468.1:c.40T>C ENSP00000458994.1:p.Tyr14His
ENST00000498155.1:c.452T>C ENSP00000417662.1:p.Leu151Pro
ENST00000529564.1:c.283+2041T>C ENSP00000431371.1:n.283+2041T>C
ENST00000532364.1:c.173+3286T>C ENSP00000460316.1:n.173+3286T>C
ENST00000533518.5:c.228T>C
NM_001311311.1:c.439T>C NP_001298240.1:p.Tyr147His
NM_024006.4:c.355T>C NP_076869.1:p.Tyr119His
NM_024006.5:c.355T>C NP_076869.1:p.Tyr119His
NM_206824.1:c.245T>C NP_996560.1:p.Leu82Pro
NM_206824.2:c.245T>C NP_996560.1:p.Leu82Pro
XM_011545944.1:c.355T>C XP_011544246.1:p.Tyr119His
XM_011545945.1:c.245T>C XP_011544247.1:p.Leu82Pro
XR_950848.1:n.1143T>C
NM_024006.6:c.355T>C MANE Select NP_076869.1:p.Tyr119His
NM_001311311.2:c.439T>C NP_001298240.1:p.Tyr147His
NM_206824.3:c.245T>C NP_996560.1:p.Leu82Pro