Canonical Allele Identifier: CA951682318

Gene: MVK

Linked Data

• dbSNP Id: rs1885850298
• gnomAD v3: 12-109594962-A-G
• gnomAD v4: 12-109594962-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109594962A>G , CM000674.2:g.109594962A>G	GRCh38
NC_000012.11:g.110032767A>G , CM000674.1:g.110032767A>G	GRCh37
NC_000012.10:g.108517150A>G	NCBI36
NG_007702.1:g.26268A>G , LRG_156:g.26268A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.43-66A>G	ENSP00000439134.1:n.43-66A>G
ENST00000546277.6:c.886-66A>G	ENSP00000438153.2:n.886-66A>G
ENST00000636529.2:n.525-66A>G
ENST00000697195.1:c.*650-66A>G	ENSP00000513181.1:n.*650-66A>G
ENST00000697196.1:c.*59-66A>G	ENSP00000513182.1:n.*59-66A>G
ENST00000697197.1:n.2915-66A>G
ENST00000697198.1:n.1204A>G
ENST00000228510.8:c.886-66A>G MANE Select	ENSP00000228510.3:n.886-66A>G
ENST00000636529.1:c.511-66A>G
ENST00000636996.1:c.734-66A>G
ENST00000228510.7:c.886-66A>G	ENSP00000228510.3:n.886-66A>G
ENST00000392727.7:c.730-66A>G	ENSP00000376487.3:n.730-66A>G
ENST00000447878.6:c.*333-66A>G	ENSP00000415555.2:n.*333-66A>G
ENST00000537237.5:c.*559-66A>G	ENSP00000445382.1:n.*559-66A>G
ENST00000539575.4:c.886-66A>G	ENSP00000443551.2:n.886-66A>G
ENST00000539696.5:c.43-66A>G	ENSP00000439134.1:n.43-66A>G
ENST00000540353.1:n.3119-66A>G
ENST00000625889.2:c.730-66A>G	ENSP00000486846.1:n.730-66A>G
ENST00000629016.2:c.*333-66A>G	ENSP00000486804.1:n.*333-66A>G
NM_000431.3:c.886-66A>G	NP_000422.1:n.886-66A>G
NM_001114185.2:c.886-66A>G	NP_001107657.1:n.886-66A>G
NM_001301182.1:c.730-66A>G	NP_001288111.1:n.730-66A>G
XM_011538372.1:c.886-66A>G	XP_011536674.1:n.886-66A>G
XM_017019313.2:c.730-66A>G	XP_016874802.1:n.730-66A>G
XM_017019314.1:c.886-66A>G	XP_016874803.1:n.886-66A>G
NM_000431.4:c.886-66A>G MANE Select	NP_000422.1:n.886-66A>G
NM_001114185.3:c.886-66A>G	NP_001107657.1:n.886-66A>G
NM_001301182.2:c.730-66A>G	NP_001288111.1:n.730-66A>G