Canonical Allele Identifier: CA2797399466

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591473_109591474insGAT , CM000674.2:g.109591473_109591474insGAT	GRCh38
NC_000012.11:g.110029278_110029279insGAT , CM000674.1:g.110029278_110029279insGAT	GRCh37
NC_000012.10:g.108513661_108513662insGAT	NCBI36
NG_007702.1:g.22779_22780insGAT , LRG_156:g.22779_22780insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+116_42+117insGAT	ENSP00000439134.1:n.42+116_42+117insGAT
ENST00000546277.6:c.885+116_885+117insGAT	ENSP00000438153.2:n.885+116_885+117insGAT
ENST00000636529.2:n.524+116_524+117insGAT
ENST00000697195.1:c.*649+116_*649+117insGAT	ENSP00000513181.1:n.*649+116_*649+117insGAT
ENST00000697196.1:c.*58+116_*58+117insGAT	ENSP00000513182.1:n.*58+116_*58+117insGAT
ENST00000697197.1:n.2914+116_2914+117insGAT
ENST00000228510.8:c.885+116_885+117insGAT MANE Select	ENSP00000228510.3:n.885+116_885+117insGAT
ENST00000636529.1:c.510+116_510+117insGAT
ENST00000636996.1:c.733+116_733+117insGAT
ENST00000228510.7:c.885+116_885+117insGAT	ENSP00000228510.3:n.885+116_885+117insGAT
ENST00000392727.7:c.729+116_729+117insGAT	ENSP00000376487.3:n.729+116_729+117insGAT
ENST00000447878.6:c.*332+116_*332+117insGAT	ENSP00000415555.2:n.*332+116_*332+117insGAT
ENST00000537237.5:c.*558+116_*558+117insGAT	ENSP00000445382.1:n.*558+116_*558+117insGAT
ENST00000539575.4:c.885+116_885+117insGAT	ENSP00000443551.2:n.885+116_885+117insGAT
ENST00000539696.5:c.42+116_42+117insGAT	ENSP00000439134.1:n.42+116_42+117insGAT
ENST00000540353.1:n.3118+116_3118+117insGAT
ENST00000625889.2:c.729+116_729+117insGAT	ENSP00000486846.1:n.729+116_729+117insGAT
ENST00000629016.2:c.*332+116_*332+117insGAT	ENSP00000486804.1:n.*332+116_*332+117insGAT
NM_000431.3:c.885+116_885+117insGAT	NP_000422.1:n.885+116_885+117insGAT
NM_001114185.2:c.885+116_885+117insGAT	NP_001107657.1:n.885+116_885+117insGAT
NM_001301182.1:c.729+116_729+117insGAT	NP_001288111.1:n.729+116_729+117insGAT
XM_011538372.1:c.885+116_885+117insGAT	XP_011536674.1:n.885+116_885+117insGAT
XM_017019313.2:c.729+116_729+117insGAT	XP_016874802.1:n.729+116_729+117insGAT
XM_017019314.1:c.885+116_885+117insGAT	XP_016874803.1:n.885+116_885+117insGAT
XM_024448982.1:c.1001_1002insGAT	XP_024304750.1:p.Asp334delinsGluIle
NM_000431.4:c.885+116_885+117insGAT MANE Select	NP_000422.1:n.885+116_885+117insGAT
NM_001114185.3:c.885+116_885+117insGAT	NP_001107657.1:n.885+116_885+117insGAT
NM_001301182.2:c.729+116_729+117insGAT	NP_001288111.1:n.729+116_729+117insGAT