Canonical Allele Identifier: CA2062438261
Gene: MVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109586192C= , CM000674.2:g.109586192C= GRCh38
NC_000012.11:g.110023997C= , CM000674.1:g.110023997C= GRCh37
NC_000012.10:g.108508380C= NCBI36
NG_007702.1:g.17498C= , LRG_156:g.17498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.-91-4654C= ENSP00000439134.1:n.-91-4654C=
ENST00000546277.6:c.631+67C= ENSP00000438153.2:n.631+67C=
ENST00000636529.2:n.182+67C=
ENST00000697195.1:c.*395+67C= ENSP00000513181.1:n.*395+67C=
ENST00000697196.1:c.631+67C= ENSP00000513182.1:n.631+67C=
ENST00000228510.8:c.631+67C= MANE Select ENSP00000228510.3:n.631+67C=
ENST00000636529.1:c.168+67C=
ENST00000636996.1:c.479+67C=
ENST00000228510.7:c.631+67C= ENSP00000228510.3:n.631+67C=
ENST00000392727.7:c.475+67C= ENSP00000376487.3:n.475+67C=
ENST00000447878.6:c.*78+67C= ENSP00000415555.2:n.*78+67C=
ENST00000537237.5:c.*395+67C= ENSP00000445382.1:n.*395+67C=
ENST00000539575.4:c.631+67C= ENSP00000443551.2:n.631+67C=
ENST00000539696.5:c.-91-4654C= ENSP00000439134.1:n.-91-4654C=
ENST00000545516.1:n.176+67C=
ENST00000545774.5:c.*78+67C= ENSP00000443978.1:n.*78+67C=
ENST00000625889.2:c.475+67C= ENSP00000486846.1:n.475+67C=
ENST00000629016.2:c.*78+67C= ENSP00000486804.1:n.*78+67C=
NM_000431.3:c.631+67C= NP_000422.1:n.631+67C=
NM_001114185.2:c.631+67C= NP_001107657.1:n.631+67C=
NM_001301182.1:c.475+67C= NP_001288111.1:n.475+67C=
XM_011538372.1:c.631+67C= XP_011536674.1:n.631+67C=
XM_017019313.2:c.475+67C= XP_016874802.1:n.475+67C=
XM_017019314.1:c.631+67C= XP_016874803.1:n.631+67C=
XM_024448982.1:c.631+67C= XP_024304750.1:n.631+67C=
NM_000431.4:c.631+67C= MANE Select NP_000422.1:n.631+67C=
NM_001114185.3:c.631+67C= NP_001107657.1:n.631+67C=
NM_001301182.2:c.475+67C= NP_001288111.1:n.475+67C=