Canonical Allele Identifier: CA386643354
Gene: MVK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109576025A>T , CM000674.2:g.109576025A>T GRCh38
NC_000012.11:g.110013830A>T , CM000674.1:g.110013830A>T GRCh37
NC_000012.10:g.108498213A>T NCBI36
NG_007096.1:g.2473T>A
NG_007702.1:g.7331A>T , LRG_156:g.7331A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000539696.6:c.-92+2152A>T ENSP00000439134.1:n.-92+2152A>T
ENST00000546277.6:c.106A>T ENSP00000438153.2:p.Arg36Ter
ENST00000636529.2:n.78+1125A>T
ENST00000697195.1:c.106A>T ENSP00000513181.1:p.Arg36Ter
ENST00000697196.1:c.106A>T ENSP00000513182.1:p.Arg36Ter
ENST00000228510.8:c.106A>T MANE Select ENSP00000228510.3:p.Arg36Ter
ENST00000636529.1:c.64+1125A>T
ENST00000636996.1:c.99A>T
ENST00000639206.1:c.106A>T ENSP00000492778.1:p.Arg36Ter
ENST00000228510.7:c.106A>T ENSP00000228510.3:p.Arg36Ter
ENST00000392727.7:c.106A>T ENSP00000376487.3:p.Arg36Ter
ENST00000447878.6:c.106A>T ENSP00000415555.2:p.Arg36Ter
ENST00000535044.1:n.351A>T
ENST00000537237.5:c.106A>T ENSP00000445382.1:p.Arg36Ter
ENST00000539335.5:c.106A>T ENSP00000440379.1:p.Arg36Ter
ENST00000539575.4:c.106A>T ENSP00000443551.2:p.Arg36Ter
ENST00000539696.5:c.-92+2152A>T ENSP00000439134.1:n.-92+2152A>T
ENST00000545774.5:c.106A>T ENSP00000443978.1:p.Arg36Ter
ENST00000546277.5:c.106A>T ENSP00000438153.1:p.Arg36Ter
ENST00000625889.2:c.106A>T ENSP00000486846.1:p.Arg36Ter
ENST00000629016.2:c.106A>T ENSP00000486804.1:p.Arg36Ter
NM_000431.3:c.106A>T NP_000422.1:p.Arg36Ter
NM_001114185.2:c.106A>T NP_001107657.1:p.Arg36Ter
NM_001301182.1:c.106A>T NP_001288111.1:p.Arg36Ter
XM_011538372.1:c.106A>T XP_011536674.1:p.Arg36Ter
XM_017019313.2:c.106A>T XP_016874802.1:p.Arg36Ter
XM_017019314.1:c.106A>T XP_016874803.1:p.Arg36Ter
XM_024448982.1:c.106A>T XP_024304750.1:p.Arg36Ter
NM_000431.4:c.106A>T MANE Select NP_000422.1:p.Arg36Ter
NM_001114185.3:c.106A>T NP_001107657.1:p.Arg36Ter
NM_001301182.2:c.106A>T NP_001288111.1:p.Arg36Ter