Canonical Allele Identifier: CA2632822617

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31093697-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093697_31093698insAA , CM000678.2:g.31093697_31093698insAA	GRCh38
NC_000016.9:g.31105018_31105019insAA , CM000678.1:g.31105018_31105019insAA	GRCh37
NC_000016.8:g.31012519_31012520insAA	NCBI36
NG_011564.1:g.6258_6259insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-277_174-276insTT MANE Select	ENSP00000378426.2:n.174-277_174-276insTT
ENST00000300851.10:c.174-216_174-215insTT	ENSP00000300851.6:n.174-216_174-215insTT
ENST00000319788.11:c.174-277_174-276insTT	ENSP00000326135.7:n.174-277_174-276insTT
ENST00000354895.4:c.173+859_173+860insTT	ENSP00000346969.4:n.173+859_173+860insTT
ENST00000394971.7:c.268-277_268-276insTT	ENSP00000378422.3:n.268-277_268-276insTT
ENST00000394975.2:c.174-277_174-276insTT	ENSP00000378426.2:n.174-277_174-276insTT
ENST00000420057.2:c.245+1691_245+1692insTT
ENST00000498155.1:c.271-277_271-276insTT	ENSP00000417662.1:n.271-277_271-276insTT
ENST00000529564.1:c.174-277_174-276insTT	ENSP00000431371.1:n.174-277_174-276insTT
ENST00000532364.1:c.173+859_173+860insTT	ENSP00000460316.1:n.173+859_173+860insTT
ENST00000533518.5:c.47-277_47-276insTT
NM_001311311.1:c.174-277_174-276insTT	NP_001298240.1:n.174-277_174-276insTT
NM_024006.4:c.174-277_174-276insTT	NP_076869.1:n.174-277_174-276insTT
NM_024006.5:c.174-277_174-276insTT	NP_076869.1:n.174-277_174-276insTT
NM_206824.1:c.173+859_173+860insTT	NP_996560.1:n.173+859_173+860insTT
NM_206824.2:c.173+859_173+860insTT	NP_996560.1:n.173+859_173+860insTT
XM_011545944.1:c.174-277_174-276insTT	XP_011544246.1:n.174-277_174-276insTT
XM_011545945.1:c.173+859_173+860insTT	XP_011544247.1:n.173+859_173+860insTT
XR_950848.1:n.962-277_962-276insTT
NM_024006.6:c.174-277_174-276insTT MANE Select	NP_076869.1:n.174-277_174-276insTT
NM_001311311.2:c.174-277_174-276insTT	NP_001298240.1:n.174-277_174-276insTT
NM_206824.3:c.173+859_173+860insTT	NP_996560.1:n.173+859_173+860insTT