Canonical Allele Identifier: CA2632822593

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31093696-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093697_31093698insCC , CM000678.2:g.31093697_31093698insCC	GRCh38
NC_000016.9:g.31105018_31105019insCC , CM000678.1:g.31105018_31105019insCC	GRCh37
NC_000016.8:g.31012519_31012520insCC	NCBI36
NG_011564.1:g.6259_6260insGG

Transcript Alleles

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