Canonical Allele Identifier: CA149804
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97577
ClinVar RCV Id: RCV000083829
dbSNP Id: rs104895328

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109574844G>C , CM000674.2:g.109574844G>C GRCh38
NC_000012.11:g.110012649G>C , CM000674.1:g.110012649G>C GRCh37
NC_000012.10:g.108497032G>C NCBI36
NG_007096.1:g.3654C>G
NG_007702.1:g.6150G>C , LRG_156:g.6150G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000539696.6:c.-92+971G>C ENSP00000439134.1:n.-92+971G>C
ENST00000546277.6:c.22G>C ENSP00000438153.2:p.Val8Leu
ENST00000636529.2:n.22G>C
ENST00000697195.1:c.22G>C ENSP00000513181.1:p.Val8Leu
ENST00000697196.1:c.22G>C ENSP00000513182.1:p.Val8Leu
ENST00000228510.8:c.22G>C MANE Select ENSP00000228510.3:p.Val8Leu
ENST00000636529.1:c.8G>C
ENST00000636996.1:c.15G>C
ENST00000639206.1:c.22G>C ENSP00000492778.1:p.Val8Leu
ENST00000228510.7:c.22G>C ENSP00000228510.3:p.Val8Leu
ENST00000392727.7:c.22G>C ENSP00000376487.3:p.Val8Leu
ENST00000447878.6:c.22G>C ENSP00000415555.2:p.Val8Leu
ENST00000535044.1:n.267G>C
ENST00000537237.5:c.22G>C ENSP00000445382.1:p.Val8Leu
ENST00000539335.5:c.22G>C ENSP00000440379.1:p.Val8Leu
ENST00000539575.4:c.22G>C ENSP00000443551.2:p.Val8Leu
ENST00000539696.5:c.-92+971G>C ENSP00000439134.1:n.-92+971G>C
ENST00000545774.5:c.22G>C ENSP00000443978.1:p.Val8Leu
ENST00000546277.5:c.22G>C ENSP00000438153.1:p.Val8Leu
ENST00000625889.2:c.22G>C ENSP00000486846.1:p.Val8Leu
ENST00000629016.2:c.22G>C ENSP00000486804.1:p.Val8Leu
NM_000431.3:c.22G>C NP_000422.1:p.Val8Leu
NM_001114185.2:c.22G>C NP_001107657.1:p.Val8Leu
NM_001301182.1:c.22G>C NP_001288111.1:p.Val8Leu
XM_011538372.1:c.22G>C XP_011536674.1:p.Val8Leu
XM_017019313.2:c.22G>C XP_016874802.1:p.Val8Leu
XM_017019314.1:c.22G>C XP_016874803.1:p.Val8Leu
XM_024448982.1:c.22G>C XP_024304750.1:p.Val8Leu
NM_000431.4:c.22G>C MANE Select NP_000422.1:p.Val8Leu
NM_001114185.3:c.22G>C NP_001107657.1:p.Val8Leu
NM_001301182.2:c.22G>C NP_001288111.1:p.Val8Leu