Canonical Allele Identifier: CA2620818507

Gene: MVK

Linked Data

• gnomAD v4: 12-109591406-C-CTTGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591406_109591407insTTGGA , CM000674.2:g.109591406_109591407insTTGGA	GRCh38
NC_000012.11:g.110029211_110029212insTTGGA , CM000674.1:g.110029211_110029212insTTGGA	GRCh37
NC_000012.10:g.108513594_108513595insTTGGA	NCBI36
NG_007702.1:g.22712_22713insTTGGA , LRG_156:g.22712_22713insTTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+49_42+50insTTGGA	ENSP00000439134.1:n.42+49_42+50insTTGGA
ENST00000546277.6:c.885+49_885+50insTTGGA	ENSP00000438153.2:n.885+49_885+50insTTGGA
ENST00000636529.2:n.524+49_524+50insTTGGA
ENST00000697195.1:c.*649+49_*649+50insTTGGA	ENSP00000513181.1:n.*649+49_*649+50insTTGGA
ENST00000697196.1:c.*58+49_*58+50insTTGGA	ENSP00000513182.1:n.*58+49_*58+50insTTGGA
ENST00000697197.1:n.2914+49_2914+50insTTGGA
ENST00000228510.8:c.885+49_885+50insTTGGA MANE Select	ENSP00000228510.3:n.885+49_885+50insTTGGA
ENST00000636529.1:c.510+49_510+50insTTGGA
ENST00000636996.1:c.733+49_733+50insTTGGA
ENST00000228510.7:c.885+49_885+50insTTGGA	ENSP00000228510.3:n.885+49_885+50insTTGGA
ENST00000392727.7:c.729+49_729+50insTTGGA	ENSP00000376487.3:n.729+49_729+50insTTGGA
ENST00000447878.6:c.*332+49_*332+50insTTGGA	ENSP00000415555.2:n.*332+49_*332+50insTTGGA
ENST00000537237.5:c.*558+49_*558+50insTTGGA	ENSP00000445382.1:n.*558+49_*558+50insTTGGA
ENST00000539575.4:c.885+49_885+50insTTGGA	ENSP00000443551.2:n.885+49_885+50insTTGGA
ENST00000539696.5:c.42+49_42+50insTTGGA	ENSP00000439134.1:n.42+49_42+50insTTGGA
ENST00000540353.1:n.3118+49_3118+50insTTGGA
ENST00000625889.2:c.729+49_729+50insTTGGA	ENSP00000486846.1:n.729+49_729+50insTTGGA
ENST00000629016.2:c.*332+49_*332+50insTTGGA	ENSP00000486804.1:n.*332+49_*332+50insTTGGA
NM_000431.3:c.885+49_885+50insTTGGA	NP_000422.1:n.885+49_885+50insTTGGA
NM_001114185.2:c.885+49_885+50insTTGGA	NP_001107657.1:n.885+49_885+50insTTGGA
NM_001301182.1:c.729+49_729+50insTTGGA	NP_001288111.1:n.729+49_729+50insTTGGA
XM_011538372.1:c.885+49_885+50insTTGGA	XP_011536674.1:n.885+49_885+50insTTGGA
XM_017019313.2:c.729+49_729+50insTTGGA	XP_016874802.1:n.729+49_729+50insTTGGA
XM_017019314.1:c.885+49_885+50insTTGGA	XP_016874803.1:n.885+49_885+50insTTGGA
XM_024448982.1:c.934_935insTTGGA	XP_024304750.1:p.Pro312LeufsTer19
NM_000431.4:c.885+49_885+50insTTGGA MANE Select	NP_000422.1:n.885+49_885+50insTTGGA
NM_001114185.3:c.885+49_885+50insTTGGA	NP_001107657.1:n.885+49_885+50insTTGGA
NM_001301182.2:c.729+49_729+50insTTGGA	NP_001288111.1:n.729+49_729+50insTTGGA