Canonical Allele Identifier: CA2620818698

Gene: MVK

Linked Data

• ClinVar Variation Id: 2940644
• ClinVar RCV Id: RCV003799954
• gnomAD v4: 12-109595021-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595021C>T , CM000674.2:g.109595021C>T	GRCh38
NC_000012.11:g.110032826C>T , CM000674.1:g.110032826C>T	GRCh37
NC_000012.10:g.108517209C>T	NCBI36
NG_007702.1:g.26327C>T , LRG_156:g.26327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.43-7C>T	ENSP00000439134.1:n.43-7C>T
ENST00000546277.6:c.886-7C>T	ENSP00000438153.2:n.886-7C>T
ENST00000636529.2:n.525-7C>T
ENST00000697195.1:c.*650-7C>T	ENSP00000513181.1:n.*650-7C>T
ENST00000697196.1:c.*59-7C>T	ENSP00000513182.1:n.*59-7C>T
ENST00000697197.1:n.2915-7C>T
ENST00000697198.1:n.1263C>T
ENST00000228510.8:c.886-7C>T MANE Select	ENSP00000228510.3:n.886-7C>T
ENST00000636529.1:c.511-7C>T
ENST00000636996.1:c.734-7C>T
ENST00000228510.7:c.886-7C>T	ENSP00000228510.3:n.886-7C>T
ENST00000392727.7:c.730-7C>T	ENSP00000376487.3:n.730-7C>T
ENST00000447878.6:c.*333-7C>T	ENSP00000415555.2:n.*333-7C>T
ENST00000537237.5:c.*559-7C>T	ENSP00000445382.1:n.*559-7C>T
ENST00000539575.4:c.886-7C>T	ENSP00000443551.2:n.886-7C>T
ENST00000539696.5:c.43-7C>T	ENSP00000439134.1:n.43-7C>T
ENST00000540353.1:n.3119-7C>T
ENST00000625889.2:c.730-7C>T	ENSP00000486846.1:n.730-7C>T
ENST00000629016.2:c.*333-7C>T	ENSP00000486804.1:n.*333-7C>T
NM_000431.3:c.886-7C>T	NP_000422.1:n.886-7C>T
NM_001114185.2:c.886-7C>T	NP_001107657.1:n.886-7C>T
NM_001301182.1:c.730-7C>T	NP_001288111.1:n.730-7C>T
XM_011538372.1:c.886-7C>T	XP_011536674.1:n.886-7C>T
XM_017019313.2:c.730-7C>T	XP_016874802.1:n.730-7C>T
XM_017019314.1:c.886-7C>T	XP_016874803.1:n.886-7C>T
NM_000431.4:c.886-7C>T MANE Select	NP_000422.1:n.886-7C>T
NM_001114185.3:c.886-7C>T	NP_001107657.1:n.886-7C>T
NM_001301182.2:c.730-7C>T	NP_001288111.1:n.730-7C>T