Canonical Allele Identifier: CA2539099434
Gene: MVK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109596043del , CM000674.2:g.109596043del GRCh38
NC_000012.11:g.110033848del , CM000674.1:g.110033848del GRCh37
NC_000012.10:g.108518231del NCBI36
NG_007702.1:g.27349del , LRG_156:g.27349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.197-383del ENSP00000439134.1:n.197-383del
ENST00000546277.6:c.1040-383del ENSP00000438153.2:n.1040-383del
ENST00000636529.2:n.679-383del
ENST00000697195.1:c.*804-383del ENSP00000513181.1:n.*804-383del
ENST00000697196.1:c.*213-383del ENSP00000513182.1:n.*213-383del
ENST00000697197.1:n.3069-383del
ENST00000697198.1:n.1424-383del
ENST00000228510.8:c.1040-383del MANE Select ENSP00000228510.3:n.1040-383del
ENST00000636529.1:c.665-383del
ENST00000636996.1:c.888-383del
ENST00000228510.7:c.1040-383del ENSP00000228510.3:n.1040-383del
ENST00000392727.7:c.884-383del ENSP00000376487.3:n.884-383del
ENST00000447878.6:c.*487-383del ENSP00000415555.2:n.*487-383del
ENST00000537237.5:c.*713-383del ENSP00000445382.1:n.*713-383del
ENST00000539575.4:c.1040-383del ENSP00000443551.2:n.1040-383del
ENST00000539696.5:c.197-383del ENSP00000439134.1:n.197-383del
ENST00000540353.1:n.3273-383del
ENST00000625889.2:c.884-383del ENSP00000486846.1:n.884-383del
ENST00000629016.2:c.*487-383del ENSP00000486804.1:n.*487-383del
NM_000431.3:c.1040-383del NP_000422.1:n.1040-383del
NM_001114185.2:c.1040-383del NP_001107657.1:n.1040-383del
NM_001301182.1:c.884-383del NP_001288111.1:n.884-383del
XM_011538372.1:c.1040-383del XP_011536674.1:n.1040-383del
XM_017019313.2:c.884-383del XP_016874802.1:n.884-383del
XM_017019314.1:c.1040-383del XP_016874803.1:n.1040-383del
NM_000431.4:c.1040-383del MANE Select NP_000422.1:n.1040-383del
NM_001114185.3:c.1040-383del NP_001107657.1:n.1040-383del
NM_001301182.2:c.884-383del NP_001288111.1:n.884-383del