Canonical Allele Identifier: CA607288971

Gene: MVK

Linked Data

• dbSNP Id: rs1566150925
• gnomAD v2: 12-110029189-GT-G
• gnomAD v4: 12-109591384-GT-G
• MyVariant Identifiers: chr12:g.110029190del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591386del , CM000674.2:g.109591386del	GRCh38
NC_000012.11:g.110029191del , CM000674.1:g.110029191del	GRCh37
NC_000012.10:g.108513574del	NCBI36
NG_007702.1:g.22692del , LRG_156:g.22692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+29del	ENSP00000439134.1:n.42+29del
ENST00000546277.6:c.885+29del	ENSP00000438153.2:n.885+29del
ENST00000636529.2:n.524+29del
ENST00000697195.1:c.*649+29del	ENSP00000513181.1:n.*649+29del
ENST00000697196.1:c.*58+29del	ENSP00000513182.1:n.*58+29del
ENST00000697197.1:n.2914+29del
ENST00000228510.8:c.885+29del MANE Select	ENSP00000228510.3:n.885+29del
ENST00000636529.1:c.510+29del
ENST00000636996.1:c.733+29del
ENST00000228510.7:c.885+29del	ENSP00000228510.3:n.885+29del
ENST00000392727.7:c.729+29del	ENSP00000376487.3:n.729+29del
ENST00000447878.6:c.*332+29del	ENSP00000415555.2:n.*332+29del
ENST00000537237.5:c.*558+29del	ENSP00000445382.1:n.*558+29del
ENST00000539575.4:c.885+29del	ENSP00000443551.2:n.885+29del
ENST00000539696.5:c.42+29del	ENSP00000439134.1:n.42+29del
ENST00000540353.1:n.3118+29del
ENST00000625889.2:c.729+29del	ENSP00000486846.1:n.729+29del
ENST00000629016.2:c.*332+29del	ENSP00000486804.1:n.*332+29del
NM_000431.3:c.885+29del	NP_000422.1:n.885+29del
NM_001114185.2:c.885+29del	NP_001107657.1:n.885+29del
NM_001301182.1:c.729+29del	NP_001288111.1:n.729+29del
XM_011538372.1:c.885+29del	XP_011536674.1:n.885+29del
XM_017019313.2:c.729+29del	XP_016874802.1:n.729+29del
XM_017019314.1:c.885+29del	XP_016874803.1:n.885+29del
XM_024448982.1:c.914del	XP_024304750.1:p.Leu305TyrfsTer2
NM_000431.4:c.885+29del MANE Select	NP_000422.1:n.885+29del
NM_001114185.3:c.885+29del	NP_001107657.1:n.885+29del
NM_001301182.2:c.729+29del	NP_001288111.1:n.729+29del