Canonical Allele Identifier: CA2632822797

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31093706-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093706_31093707insC , CM000678.2:g.31093706_31093707insC	GRCh38
NC_000016.9:g.31105027_31105028insC , CM000678.1:g.31105027_31105028insC	GRCh37
NC_000016.8:g.31012528_31012529insC	NCBI36
NG_011564.1:g.6249_6250insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-286_174-285insG MANE Select	ENSP00000378426.2:n.174-286_174-285insG
ENST00000300851.10:c.174-225_174-224insG	ENSP00000300851.6:n.174-225_174-224insG
ENST00000319788.11:c.174-286_174-285insG	ENSP00000326135.7:n.174-286_174-285insG
ENST00000354895.4:c.173+850_173+851insG	ENSP00000346969.4:n.173+850_173+851insG
ENST00000394971.7:c.268-286_268-285insG	ENSP00000378422.3:n.268-286_268-285insG
ENST00000394975.2:c.174-286_174-285insG	ENSP00000378426.2:n.174-286_174-285insG
ENST00000420057.2:c.245+1682_245+1683insG
ENST00000498155.1:c.271-286_271-285insG	ENSP00000417662.1:n.271-286_271-285insG
ENST00000529564.1:c.174-286_174-285insG	ENSP00000431371.1:n.174-286_174-285insG
ENST00000532364.1:c.173+850_173+851insG	ENSP00000460316.1:n.173+850_173+851insG
ENST00000533518.5:c.47-286_47-285insG
NM_001311311.1:c.174-286_174-285insG	NP_001298240.1:n.174-286_174-285insG
NM_024006.4:c.174-286_174-285insG	NP_076869.1:n.174-286_174-285insG
NM_024006.5:c.174-286_174-285insG	NP_076869.1:n.174-286_174-285insG
NM_206824.1:c.173+850_173+851insG	NP_996560.1:n.173+850_173+851insG
NM_206824.2:c.173+850_173+851insG	NP_996560.1:n.173+850_173+851insG
XM_011545944.1:c.174-286_174-285insG	XP_011544246.1:n.174-286_174-285insG
XM_011545945.1:c.173+850_173+851insG	XP_011544247.1:n.173+850_173+851insG
XR_950848.1:n.962-286_962-285insG
NM_024006.6:c.174-286_174-285insG MANE Select	NP_076869.1:n.174-286_174-285insG
NM_001311311.2:c.174-286_174-285insG	NP_001298240.1:n.174-286_174-285insG
NM_206824.3:c.173+850_173+851insG	NP_996560.1:n.173+850_173+851insG