Canonical Allele Identifier: CA2062437907

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109586010_109586014delinsCTGTG , CM000674.2:g.109586010_109586014delinsCTGTG	GRCh38
NC_000012.11:g.110023815_110023819delinsCTGTG , CM000674.1:g.110023815_110023819delinsCTGTG	GRCh37
NC_000012.10:g.108508198_108508202delinsCTGTG	NCBI36
NG_007702.1:g.17316_17320delinsCTGTG , LRG_156:g.17316_17320delinsCTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-91-4836_-91-4832delinsCTGTG	ENSP00000439134.1:n.-91-4836_-91-4832delinsCTGTG
ENST00000546277.6:c.528-12_528-8delinsCTGTG	ENSP00000438153.2:n.528-12_528-8delinsCTGTG
ENST00000636529.2:n.79-12_79-8delinsCTGTG
ENST00000697195.1:c.*292-12_*292-8delinsCTGTG	ENSP00000513181.1:n.*292-12_*292-8delinsCTGTG
ENST00000697196.1:c.528-12_528-8delinsCTGTG	ENSP00000513182.1:n.528-12_528-8delinsCTGTG
ENST00000228510.8:c.528-12_528-8delinsCTGTG MANE Select	ENSP00000228510.3:n.528-12_528-8delinsCTGTG
ENST00000636529.1:c.65-12_65-8delinsCTGTG
ENST00000636996.1:c.376-12_376-8delinsCTGTG
ENST00000228510.7:c.528-12_528-8delinsCTGTG	ENSP00000228510.3:n.528-12_528-8delinsCTGTG
ENST00000392727.7:c.372-12_372-8delinsCTGTG	ENSP00000376487.3:n.372-12_372-8delinsCTGTG
ENST00000447878.6:c.227-12_227-8delinsCTGTG	ENSP00000415555.2:n.227-12_227-8delinsCTGTG
ENST00000535044.1:n.472-12_472-8delinsCTGTG
ENST00000537237.5:c.*292-12_*292-8delinsCTGTG	ENSP00000445382.1:n.*292-12_*292-8delinsCTGTG
ENST00000539575.4:c.528-12_528-8delinsCTGTG	ENSP00000443551.2:n.528-12_528-8delinsCTGTG
ENST00000539696.5:c.-91-4836_-91-4832delinsCTGTG	ENSP00000439134.1:n.-91-4836_-91-4832delinsCTGTG
ENST00000545516.1:n.73-12_73-8delinsCTGTG
ENST00000545774.5:c.227-12_227-8delinsCTGTG	ENSP00000443978.1:n.227-12_227-8delinsCTGTG
ENST00000546277.5:c.528-12_528-8delinsCTGTG	ENSP00000438153.1:n.528-12_528-8delinsCTGTG
ENST00000625889.2:c.372-12_372-8delinsCTGTG	ENSP00000486846.1:n.372-12_372-8delinsCTGTG
ENST00000629016.2:c.227-12_227-8delinsCTGTG	ENSP00000486804.1:n.227-12_227-8delinsCTGTG
NM_000431.3:c.528-12_528-8delinsCTGTG	NP_000422.1:n.528-12_528-8delinsCTGTG
NM_001114185.2:c.528-12_528-8delinsCTGTG	NP_001107657.1:n.528-12_528-8delinsCTGTG
NM_001301182.1:c.372-12_372-8delinsCTGTG	NP_001288111.1:n.372-12_372-8delinsCTGTG
XM_011538372.1:c.528-12_528-8delinsCTGTG	XP_011536674.1:n.528-12_528-8delinsCTGTG
XM_017019313.2:c.372-12_372-8delinsCTGTG	XP_016874802.1:n.372-12_372-8delinsCTGTG
XM_017019314.1:c.528-12_528-8delinsCTGTG	XP_016874803.1:n.528-12_528-8delinsCTGTG
XM_024448982.1:c.528-12_528-8delinsCTGTG	XP_024304750.1:n.528-12_528-8delinsCTGTG
NM_000431.4:c.528-12_528-8delinsCTGTG MANE Select	NP_000422.1:n.528-12_528-8delinsCTGTG
NM_001114185.3:c.528-12_528-8delinsCTGTG	NP_001107657.1:n.528-12_528-8delinsCTGTG
NM_001301182.2:c.372-12_372-8delinsCTGTG	NP_001288111.1:n.372-12_372-8delinsCTGTG