Canonical Allele Identifier: CA2632822590

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31093696-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093697_31093698insAC , CM000678.2:g.31093697_31093698insAC	GRCh38
NC_000016.9:g.31105018_31105019insAC , CM000678.1:g.31105018_31105019insAC	GRCh37
NC_000016.8:g.31012519_31012520insAC	NCBI36
NG_011564.1:g.6259_6260insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-276_174-275insTG MANE Select	ENSP00000378426.2:n.174-276_174-275insTG
ENST00000300851.10:c.174-215_174-214insTG	ENSP00000300851.6:n.174-215_174-214insTG
ENST00000319788.11:c.174-276_174-275insTG	ENSP00000326135.7:n.174-276_174-275insTG
ENST00000354895.4:c.173+860_173+861insTG	ENSP00000346969.4:n.173+860_173+861insTG
ENST00000394971.7:c.268-276_268-275insTG	ENSP00000378422.3:n.268-276_268-275insTG
ENST00000394975.2:c.174-276_174-275insTG	ENSP00000378426.2:n.174-276_174-275insTG
ENST00000420057.2:c.245+1692_245+1693insTG
ENST00000498155.1:c.271-276_271-275insTG	ENSP00000417662.1:n.271-276_271-275insTG
ENST00000529564.1:c.174-276_174-275insTG	ENSP00000431371.1:n.174-276_174-275insTG
ENST00000532364.1:c.173+860_173+861insTG	ENSP00000460316.1:n.173+860_173+861insTG
ENST00000533518.5:c.47-276_47-275insTG
NM_001311311.1:c.174-276_174-275insTG	NP_001298240.1:n.174-276_174-275insTG
NM_024006.4:c.174-276_174-275insTG	NP_076869.1:n.174-276_174-275insTG
NM_024006.5:c.174-276_174-275insTG	NP_076869.1:n.174-276_174-275insTG
NM_206824.1:c.173+860_173+861insTG	NP_996560.1:n.173+860_173+861insTG
NM_206824.2:c.173+860_173+861insTG	NP_996560.1:n.173+860_173+861insTG
XM_011545944.1:c.174-276_174-275insTG	XP_011544246.1:n.174-276_174-275insTG
XM_011545945.1:c.173+860_173+861insTG	XP_011544247.1:n.173+860_173+861insTG
XR_950848.1:n.962-276_962-275insTG
NM_024006.6:c.174-276_174-275insTG MANE Select	NP_076869.1:n.174-276_174-275insTG
NM_001311311.2:c.174-276_174-275insTG	NP_001298240.1:n.174-276_174-275insTG
NM_206824.3:c.173+860_173+861insTG	NP_996560.1:n.173+860_173+861insTG