Canonical Allele Identifier: CA2620818519

Gene: MVK

Linked Data

• gnomAD v4: 12-109591417-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591418_109591420del , CM000674.2:g.109591418_109591420del	GRCh38
NC_000012.11:g.110029223_110029225del , CM000674.1:g.110029223_110029225del	GRCh37
NC_000012.10:g.108513606_108513608del	NCBI36
NG_007702.1:g.22724_22726del , LRG_156:g.22724_22726del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+61_42+63del	ENSP00000439134.1:n.42+61_42+63del
ENST00000546277.6:c.885+61_885+63del	ENSP00000438153.2:n.885+61_885+63del
ENST00000636529.2:n.524+61_524+63del
ENST00000697195.1:c.*649+61_*649+63del	ENSP00000513181.1:n.*649+61_*649+63del
ENST00000697196.1:c.*58+61_*58+63del	ENSP00000513182.1:n.*58+61_*58+63del
ENST00000697197.1:n.2914+61_2914+63del
ENST00000228510.8:c.885+61_885+63del MANE Select	ENSP00000228510.3:n.885+61_885+63del
ENST00000636529.1:c.510+61_510+63del
ENST00000636996.1:c.733+61_733+63del
ENST00000228510.7:c.885+61_885+63del	ENSP00000228510.3:n.885+61_885+63del
ENST00000392727.7:c.729+61_729+63del	ENSP00000376487.3:n.729+61_729+63del
ENST00000447878.6:c.*332+61_*332+63del	ENSP00000415555.2:n.*332+61_*332+63del
ENST00000537237.5:c.*558+61_*558+63del	ENSP00000445382.1:n.*558+61_*558+63del
ENST00000539575.4:c.885+61_885+63del	ENSP00000443551.2:n.885+61_885+63del
ENST00000539696.5:c.42+61_42+63del	ENSP00000439134.1:n.42+61_42+63del
ENST00000540353.1:n.3118+61_3118+63del
ENST00000625889.2:c.729+61_729+63del	ENSP00000486846.1:n.729+61_729+63del
ENST00000629016.2:c.*332+61_*332+63del	ENSP00000486804.1:n.*332+61_*332+63del
NM_000431.3:c.885+61_885+63del	NP_000422.1:n.885+61_885+63del
NM_001114185.2:c.885+61_885+63del	NP_001107657.1:n.885+61_885+63del
NM_001301182.1:c.729+61_729+63del	NP_001288111.1:n.729+61_729+63del
XM_011538372.1:c.885+61_885+63del	XP_011536674.1:n.885+61_885+63del
XM_017019313.2:c.729+61_729+63del	XP_016874802.1:n.729+61_729+63del
XM_017019314.1:c.885+61_885+63del	XP_016874803.1:n.885+61_885+63del
XM_024448982.1:c.946_948del	XP_024304750.1:p.Leu316del
NM_000431.4:c.885+61_885+63del MANE Select	NP_000422.1:n.885+61_885+63del
NM_001114185.3:c.885+61_885+63del	NP_001107657.1:n.885+61_885+63del
NM_001301182.2:c.729+61_729+63del	NP_001288111.1:n.729+61_729+63del