Canonical Allele Identifier: CA2797399432
Gene: MVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109591432_109591433insA , CM000674.2:g.109591432_109591433insA GRCh38
NC_000012.11:g.110029237_110029238insA , CM000674.1:g.110029237_110029238insA GRCh37
NC_000012.10:g.108513620_108513621insA NCBI36
NG_007702.1:g.22738_22739insA , LRG_156:g.22738_22739insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.42+75_42+76insA ENSP00000439134.1:n.42+75_42+76insA
ENST00000546277.6:c.885+75_885+76insA ENSP00000438153.2:n.885+75_885+76insA
ENST00000636529.2:n.524+75_524+76insA
ENST00000697195.1:c.*649+75_*649+76insA ENSP00000513181.1:n.*649+75_*649+76insA
ENST00000697196.1:c.*58+75_*58+76insA ENSP00000513182.1:n.*58+75_*58+76insA
ENST00000697197.1:n.2914+75_2914+76insA
ENST00000228510.8:c.885+75_885+76insA MANE Select ENSP00000228510.3:n.885+75_885+76insA
ENST00000636529.1:c.510+75_510+76insA
ENST00000636996.1:c.733+75_733+76insA
ENST00000228510.7:c.885+75_885+76insA ENSP00000228510.3:n.885+75_885+76insA
ENST00000392727.7:c.729+75_729+76insA ENSP00000376487.3:n.729+75_729+76insA
ENST00000447878.6:c.*332+75_*332+76insA ENSP00000415555.2:n.*332+75_*332+76insA
ENST00000537237.5:c.*558+75_*558+76insA ENSP00000445382.1:n.*558+75_*558+76insA
ENST00000539575.4:c.885+75_885+76insA ENSP00000443551.2:n.885+75_885+76insA
ENST00000539696.5:c.42+75_42+76insA ENSP00000439134.1:n.42+75_42+76insA
ENST00000540353.1:n.3118+75_3118+76insA
ENST00000625889.2:c.729+75_729+76insA ENSP00000486846.1:n.729+75_729+76insA
ENST00000629016.2:c.*332+75_*332+76insA ENSP00000486804.1:n.*332+75_*332+76insA
NM_000431.3:c.885+75_885+76insA NP_000422.1:n.885+75_885+76insA
NM_001114185.2:c.885+75_885+76insA NP_001107657.1:n.885+75_885+76insA
NM_001301182.1:c.729+75_729+76insA NP_001288111.1:n.729+75_729+76insA
XM_011538372.1:c.885+75_885+76insA XP_011536674.1:n.885+75_885+76insA
XM_017019313.2:c.729+75_729+76insA XP_016874802.1:n.729+75_729+76insA
XM_017019314.1:c.885+75_885+76insA XP_016874803.1:n.885+75_885+76insA
XM_024448982.1:c.960_961insA XP_024304750.1:p.Val321SerfsTer11
NM_000431.4:c.885+75_885+76insA MANE Select NP_000422.1:n.885+75_885+76insA
NM_001114185.3:c.885+75_885+76insA NP_001107657.1:n.885+75_885+76insA
NM_001301182.2:c.729+75_729+76insA NP_001288111.1:n.729+75_729+76insA