Canonical Allele Identifier: CA2797412177

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109575037_109575038insCT , CM000674.2:g.109575037_109575038insCT	GRCh38
NC_000012.11:g.110012842_110012843insCT , CM000674.1:g.110012842_110012843insCT	GRCh37
NC_000012.10:g.108497225_108497226insCT	NCBI36
NG_007096.1:g.3460_3461insAG
NG_007702.1:g.6343_6344insCT , LRG_156:g.6343_6344insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-92+1164_-92+1165insCT	ENSP00000439134.1:n.-92+1164_-92+1165insCT
ENST00000546277.6:c.78+137_78+138insCT	ENSP00000438153.2:n.78+137_78+138insCT
ENST00000636529.2:n.78+137_78+138insCT
ENST00000697195.1:c.78+137_78+138insCT	ENSP00000513181.1:n.78+137_78+138insCT
ENST00000697196.1:c.78+137_78+138insCT	ENSP00000513182.1:n.78+137_78+138insCT
ENST00000228510.8:c.78+137_78+138insCT MANE Select	ENSP00000228510.3:n.78+137_78+138insCT
ENST00000636529.1:c.64+137_64+138insCT
ENST00000636996.1:c.71+137_71+138insCT
ENST00000639206.1:c.78+137_78+138insCT	ENSP00000492778.1:n.78+137_78+138insCT
ENST00000228510.7:c.78+137_78+138insCT	ENSP00000228510.3:n.78+137_78+138insCT
ENST00000392727.7:c.78+137_78+138insCT	ENSP00000376487.3:n.78+137_78+138insCT
ENST00000447878.6:c.78+137_78+138insCT	ENSP00000415555.2:n.78+137_78+138insCT
ENST00000535044.1:n.323+137_323+138insCT
ENST00000537237.5:c.78+137_78+138insCT	ENSP00000445382.1:n.78+137_78+138insCT
ENST00000539335.5:c.78+137_78+138insCT	ENSP00000440379.1:n.78+137_78+138insCT
ENST00000539575.4:c.78+137_78+138insCT	ENSP00000443551.2:n.78+137_78+138insCT
ENST00000539696.5:c.-92+1164_-92+1165insCT	ENSP00000439134.1:n.-92+1164_-92+1165insCT
ENST00000545774.5:c.78+137_78+138insCT	ENSP00000443978.1:n.78+137_78+138insCT
ENST00000546277.5:c.78+137_78+138insCT	ENSP00000438153.1:n.78+137_78+138insCT
ENST00000625889.2:c.78+137_78+138insCT	ENSP00000486846.1:n.78+137_78+138insCT
ENST00000629016.2:c.78+137_78+138insCT	ENSP00000486804.1:n.78+137_78+138insCT
NM_000431.3:c.78+137_78+138insCT	NP_000422.1:n.78+137_78+138insCT
NM_001114185.2:c.78+137_78+138insCT	NP_001107657.1:n.78+137_78+138insCT
NM_001301182.1:c.78+137_78+138insCT	NP_001288111.1:n.78+137_78+138insCT
XM_011538372.1:c.78+137_78+138insCT	XP_011536674.1:n.78+137_78+138insCT
XM_017019313.2:c.78+137_78+138insCT	XP_016874802.1:n.78+137_78+138insCT
XM_017019314.1:c.78+137_78+138insCT	XP_016874803.1:n.78+137_78+138insCT
XM_024448982.1:c.78+137_78+138insCT	XP_024304750.1:n.78+137_78+138insCT
NM_000431.4:c.78+137_78+138insCT MANE Select	NP_000422.1:n.78+137_78+138insCT
NM_001114185.3:c.78+137_78+138insCT	NP_001107657.1:n.78+137_78+138insCT
NM_001301182.2:c.78+137_78+138insCT	NP_001288111.1:n.78+137_78+138insCT