Canonical Allele Identifier: CA2797413981

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109586240_109586241insGTC , CM000674.2:g.109586240_109586241insGTC	GRCh38
NC_000012.11:g.110024045_110024046insGTC , CM000674.1:g.110024045_110024046insGTC	GRCh37
NC_000012.10:g.108508428_108508429insGTC	NCBI36
NG_007702.1:g.17546_17547insGTC , LRG_156:g.17546_17547insGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-91-4606_-91-4605insGTC	ENSP00000439134.1:n.-91-4606_-91-4605insGTC
ENST00000546277.6:c.631+115_631+116insGTC	ENSP00000438153.2:n.631+115_631+116insGTC
ENST00000636529.2:n.182+115_182+116insGTC
ENST00000697195.1:c.*395+115_*395+116insGTC	ENSP00000513181.1:n.*395+115_*395+116insGTC
ENST00000697196.1:c.631+115_631+116insGTC	ENSP00000513182.1:n.631+115_631+116insGTC
ENST00000228510.8:c.631+115_631+116insGTC MANE Select	ENSP00000228510.3:n.631+115_631+116insGTC
ENST00000636529.1:c.168+115_168+116insGTC
ENST00000636996.1:c.479+115_479+116insGTC
ENST00000228510.7:c.631+115_631+116insGTC	ENSP00000228510.3:n.631+115_631+116insGTC
ENST00000392727.7:c.475+115_475+116insGTC	ENSP00000376487.3:n.475+115_475+116insGTC
ENST00000447878.6:c.*78+115_*78+116insGTC	ENSP00000415555.2:n.*78+115_*78+116insGTC
ENST00000537237.5:c.*395+115_*395+116insGTC	ENSP00000445382.1:n.*395+115_*395+116insGTC
ENST00000539575.4:c.631+115_631+116insGTC	ENSP00000443551.2:n.631+115_631+116insGTC
ENST00000539696.5:c.-91-4606_-91-4605insGTC	ENSP00000439134.1:n.-91-4606_-91-4605insGTC
ENST00000545516.1:n.176+115_176+116insGTC
ENST00000545774.5:c.*78+115_*78+116insGTC	ENSP00000443978.1:n.*78+115_*78+116insGTC
ENST00000625889.2:c.475+115_475+116insGTC	ENSP00000486846.1:n.475+115_475+116insGTC
ENST00000629016.2:c.*78+115_*78+116insGTC	ENSP00000486804.1:n.*78+115_*78+116insGTC
NM_000431.3:c.631+115_631+116insGTC	NP_000422.1:n.631+115_631+116insGTC
NM_001114185.2:c.631+115_631+116insGTC	NP_001107657.1:n.631+115_631+116insGTC
NM_001301182.1:c.475+115_475+116insGTC	NP_001288111.1:n.475+115_475+116insGTC
XM_011538372.1:c.631+115_631+116insGTC	XP_011536674.1:n.631+115_631+116insGTC
XM_017019313.2:c.475+115_475+116insGTC	XP_016874802.1:n.475+115_475+116insGTC
XM_017019314.1:c.631+115_631+116insGTC	XP_016874803.1:n.631+115_631+116insGTC
XM_024448982.1:c.631+115_631+116insGTC	XP_024304750.1:n.631+115_631+116insGTC
NM_000431.4:c.631+115_631+116insGTC MANE Select	NP_000422.1:n.631+115_631+116insGTC
NM_001114185.3:c.631+115_631+116insGTC	NP_001107657.1:n.631+115_631+116insGTC
NM_001301182.2:c.475+115_475+116insGTC	NP_001288111.1:n.475+115_475+116insGTC