Canonical Allele Identifier: CA2797399575

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591600_109591601insAGT , CM000674.2:g.109591600_109591601insAGT	GRCh38
NC_000012.11:g.110029405_110029406insAGT , CM000674.1:g.110029405_110029406insAGT	GRCh37
NC_000012.10:g.108513788_108513789insAGT	NCBI36
NG_007702.1:g.22906_22907insAGT , LRG_156:g.22906_22907insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+243_42+244insAGT	ENSP00000439134.1:n.42+243_42+244insAGT
ENST00000546277.6:c.885+243_885+244insAGT	ENSP00000438153.2:n.885+243_885+244insAGT
ENST00000636529.2:n.524+243_524+244insAGT
ENST00000697195.1:c.*649+243_*649+244insAGT	ENSP00000513181.1:n.*649+243_*649+244insAGT
ENST00000697196.1:c.*58+243_*58+244insAGT	ENSP00000513182.1:n.*58+243_*58+244insAGT
ENST00000697197.1:n.2914+243_2914+244insAGT
ENST00000228510.8:c.885+243_885+244insAGT MANE Select	ENSP00000228510.3:n.885+243_885+244insAGT
ENST00000636529.1:c.510+243_510+244insAGT
ENST00000636996.1:c.733+243_733+244insAGT
ENST00000228510.7:c.885+243_885+244insAGT	ENSP00000228510.3:n.885+243_885+244insAGT
ENST00000392727.7:c.729+243_729+244insAGT	ENSP00000376487.3:n.729+243_729+244insAGT
ENST00000447878.6:c.*332+243_*332+244insAGT	ENSP00000415555.2:n.*332+243_*332+244insAGT
ENST00000537237.5:c.*558+243_*558+244insAGT	ENSP00000445382.1:n.*558+243_*558+244insAGT
ENST00000539575.4:c.885+243_885+244insAGT	ENSP00000443551.2:n.885+243_885+244insAGT
ENST00000539696.5:c.42+243_42+244insAGT	ENSP00000439134.1:n.42+243_42+244insAGT
ENST00000540353.1:n.3118+243_3118+244insAGT
ENST00000625889.2:c.729+243_729+244insAGT	ENSP00000486846.1:n.729+243_729+244insAGT
ENST00000629016.2:c.*332+243_*332+244insAGT	ENSP00000486804.1:n.*332+243_*332+244insAGT
NM_000431.3:c.885+243_885+244insAGT	NP_000422.1:n.885+243_885+244insAGT
NM_001114185.2:c.885+243_885+244insAGT	NP_001107657.1:n.885+243_885+244insAGT
NM_001301182.1:c.729+243_729+244insAGT	NP_001288111.1:n.729+243_729+244insAGT
XM_011538372.1:c.885+243_885+244insAGT	XP_011536674.1:n.885+243_885+244insAGT
XM_017019313.2:c.729+243_729+244insAGT	XP_016874802.1:n.729+243_729+244insAGT
XM_017019314.1:c.885+243_885+244insAGT	XP_016874803.1:n.885+243_885+244insAGT
XM_024448982.1:c.1128_1129insAGT	XP_024304750.1:p.Trp376_Leu377insSer
NM_000431.4:c.885+243_885+244insAGT MANE Select	NP_000422.1:n.885+243_885+244insAGT
NM_001114185.3:c.885+243_885+244insAGT	NP_001107657.1:n.885+243_885+244insAGT
NM_001301182.2:c.729+243_729+244insAGT	NP_001288111.1:n.729+243_729+244insAGT