Canonical Allele Identifier: CA2216892928

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31093851_31093852delinsCA , CM000678.2:g.31093851_31093852delinsCA	GRCh38
NC_000016.9:g.31105172_31105173delinsCA , CM000678.1:g.31105172_31105173delinsCA	GRCh37
NC_000016.8:g.31012673_31012674delinsCA	NCBI36
NG_011564.1:g.6104_6105delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.174-431_174-430delinsTG MANE Select	ENSP00000378426.2:n.174-431_174-430delinsTG
ENST00000300851.10:c.174-370_174-369delinsTG	ENSP00000300851.6:n.174-370_174-369delinsTG
ENST00000319788.11:c.174-431_174-430delinsTG	ENSP00000326135.7:n.174-431_174-430delinsTG
ENST00000354895.4:c.173+705_173+706delinsTG	ENSP00000346969.4:n.173+705_173+706delinsTG
ENST00000394971.7:c.267+383_267+384delinsTG	ENSP00000378422.3:n.267+383_267+384delinsTG
ENST00000394975.2:c.174-431_174-430delinsTG	ENSP00000378426.2:n.174-431_174-430delinsTG
ENST00000420057.2:c.245+1537_245+1538delinsTG
ENST00000498155.1:c.271-431_271-430delinsTG	ENSP00000417662.1:n.271-431_271-430delinsTG
ENST00000529564.1:c.174-431_174-430delinsTG	ENSP00000431371.1:n.174-431_174-430delinsTG
ENST00000532364.1:c.173+705_173+706delinsTG	ENSP00000460316.1:n.173+705_173+706delinsTG
ENST00000533518.5:c.47-431_47-430delinsTG
NM_001311311.1:c.174-431_174-430delinsTG	NP_001298240.1:n.174-431_174-430delinsTG
NM_024006.4:c.174-431_174-430delinsTG	NP_076869.1:n.174-431_174-430delinsTG
NM_024006.5:c.174-431_174-430delinsTG	NP_076869.1:n.174-431_174-430delinsTG
NM_206824.1:c.173+705_173+706delinsTG	NP_996560.1:n.173+705_173+706delinsTG
NM_206824.2:c.173+705_173+706delinsTG	NP_996560.1:n.173+705_173+706delinsTG
XM_011545944.1:c.174-431_174-430delinsTG	XP_011544246.1:n.174-431_174-430delinsTG
XM_011545945.1:c.173+705_173+706delinsTG	XP_011544247.1:n.173+705_173+706delinsTG
XR_950848.1:n.962-431_962-430delinsTG
NM_024006.6:c.174-431_174-430delinsTG MANE Select	NP_076869.1:n.174-431_174-430delinsTG
NM_001311311.2:c.174-431_174-430delinsTG	NP_001298240.1:n.174-431_174-430delinsTG
NM_206824.3:c.173+705_173+706delinsTG	NP_996560.1:n.173+705_173+706delinsTG