Canonical Allele Identifier: CA481713874
Gene: MVK HGNC NCBI

Linked Data

dbSNP Id: rs1885422070
MyVariant Identifiers: chr12:g.110023920C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109586115C>A , CM000674.2:g.109586115C>A GRCh38
NC_000012.11:g.110023920C>A , CM000674.1:g.110023920C>A GRCh37
NC_000012.10:g.108508303C>A NCBI36
NG_007702.1:g.17421C>A , LRG_156:g.17421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.-91-4731C>A ENSP00000439134.1:n.-91-4731C>A
ENST00000546277.6:c.621C>A ENSP00000438153.2:p.Val207=
ENST00000636529.2:n.172C>A
ENST00000697195.1:c.*385C>A ENSP00000513181.1:n.*385C>A
ENST00000697196.1:c.621C>A ENSP00000513182.1:p.Val207=
ENST00000228510.8:c.621C>A MANE Select ENSP00000228510.3:p.Val207=
ENST00000636529.1:c.158C>A
ENST00000636996.1:c.469C>A
ENST00000228510.7:c.621C>A ENSP00000228510.3:p.Val207=
ENST00000392727.7:c.465C>A ENSP00000376487.3:p.Val155=
ENST00000447878.6:c.*68C>A ENSP00000415555.2:n.*68C>A
ENST00000537237.5:c.*385C>A ENSP00000445382.1:n.*385C>A
ENST00000539575.4:c.621C>A ENSP00000443551.2:p.Val207=
ENST00000539696.5:c.-91-4731C>A ENSP00000439134.1:n.-91-4731C>A
ENST00000545516.1:n.166C>A
ENST00000545774.5:c.*68C>A ENSP00000443978.1:n.*68C>A
ENST00000625889.2:c.465C>A ENSP00000486846.1:p.Val155=
ENST00000629016.2:c.*68C>A ENSP00000486804.1:n.*68C>A
NM_000431.3:c.621C>A NP_000422.1:p.Val207=
NM_001114185.2:c.621C>A NP_001107657.1:p.Val207=
NM_001301182.1:c.465C>A NP_001288111.1:p.Val155=
XM_011538372.1:c.621C>A XP_011536674.1:p.Val207=
XM_017019313.2:c.465C>A XP_016874802.1:p.Val155=
XM_017019314.1:c.621C>A XP_016874803.1:p.Val207=
XM_024448982.1:c.621C>A XP_024304750.1:p.Val207=
NM_000431.4:c.621C>A MANE Select NP_000422.1:p.Val207=
NM_001114185.3:c.621C>A NP_001107657.1:p.Val207=
NM_001301182.2:c.465C>A NP_001288111.1:p.Val155=