Canonical Allele Identifier: CA658683791

Gene: MVK

Linked Data

• ClinVar Variation Id: 488556
• ClinVar RCV Id: RCV000578362
• dbSNP Id: rs1295630463
• MyVariant Identifiers: chr12:g.110028670A>G (hg19) ; chr12:g.109590865A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109590865A>G , CM000674.2:g.109590865A>G	GRCh38
NC_000012.11:g.110028670A>G , CM000674.1:g.110028670A>G	GRCh37
NC_000012.10:g.108513053A>G	NCBI36
NG_007702.1:g.22171A>G , LRG_156:g.22171A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-76+4A>G	ENSP00000439134.1:n.-76+4A>G
ENST00000546277.6:c.768+4A>G	ENSP00000438153.2:n.768+4A>G
ENST00000636529.2:n.407+4A>G
ENST00000697195.1:c.*532+4A>G	ENSP00000513181.1:n.*532+4A>G
ENST00000697196.1:c.856+4A>G	ENSP00000513182.1:n.856+4A>G
ENST00000697197.1:n.2422A>G
ENST00000228510.8:c.768+4A>G MANE Select	ENSP00000228510.3:n.768+4A>G
ENST00000636529.1:c.393+4A>G
ENST00000636996.1:c.616+4A>G
ENST00000228510.7:c.768+4A>G	ENSP00000228510.3:n.768+4A>G
ENST00000392727.7:c.612+4A>G	ENSP00000376487.3:n.612+4A>G
ENST00000447878.6:c.*215+4A>G	ENSP00000415555.2:n.*215+4A>G
ENST00000537237.5:c.*442-376A>G	ENSP00000445382.1:n.*442-376A>G
ENST00000539575.4:c.768+4A>G	ENSP00000443551.2:n.768+4A>G
ENST00000539696.5:c.-76+4A>G	ENSP00000439134.1:n.-76+4A>G
ENST00000540353.1:n.3001+4A>G
ENST00000625889.2:c.612+4A>G	ENSP00000486846.1:n.612+4A>G
ENST00000629016.2:c.*215+4A>G	ENSP00000486804.1:n.*215+4A>G
NM_000431.3:c.768+4A>G	NP_000422.1:n.768+4A>G
NM_001114185.2:c.768+4A>G	NP_001107657.1:n.768+4A>G
NM_001301182.1:c.612+4A>G	NP_001288111.1:n.612+4A>G
XM_011538372.1:c.768+4A>G	XP_011536674.1:n.768+4A>G
XM_017019313.2:c.612+4A>G	XP_016874802.1:n.612+4A>G
XM_017019314.1:c.768+4A>G	XP_016874803.1:n.768+4A>G
XM_024448982.1:c.768+4A>G	XP_024304750.1:n.768+4A>G
NM_000431.4:c.768+4A>G MANE Select	NP_000422.1:n.768+4A>G
NM_001114185.3:c.768+4A>G	NP_001107657.1:n.768+4A>G
NM_001301182.2:c.612+4A>G	NP_001288111.1:n.612+4A>G