Canonical Allele Identifier: CA249734
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110800746G>A , CM000671.2:g.110800746G>A GRCh38
NC_000009.11:g.113563026G>A , CM000671.1:g.113563026G>A GRCh37
NC_000009.10:g.112602847G>A NCBI36
NG_016016.1:g.136976G>A
NG_016016.2:g.136956G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.2368G>A MANE Select ENSP00000363571.4:p.Val790Met
ENST00000189978.10:c.2110G>A ENSP00000189978.6:p.Val704Met
ENST00000374440.7:c.2110G>A ENSP00000363563.4:p.Val704Met
ENST00000374448.8:c.2368G>A ENSP00000363571.4:p.Val790Met
ENST00000416899.7:c.2344G>A ENSP00000393608.3:p.Val782Met
NM_001166280.1:c.2110G>A NP_001159752.1:p.Val704Met
NM_001166281.1:c.2080G>A NP_001159753.1:p.Val694Met
NM_005592.3:c.2368G>A NP_005583.1:p.Val790Met
XM_005251994.2:c.2398G>A XP_005252051.1:p.Val800Met
XM_005251995.2:c.2374G>A XP_005252052.1:p.Val792Met
XM_005251996.2:c.2344G>A XP_005252053.1:p.Val782Met
XM_011518707.1:c.2428G>A XP_011517009.1:p.Val810Met
XM_011518708.1:c.1132G>A XP_011517010.1:p.Val378Met
XM_005251994.3:c.2398G>A XP_005252051.1:p.Val800Met
XM_005251995.3:c.2374G>A XP_005252052.1:p.Val792Met
XM_005251996.3:c.2344G>A XP_005252053.1:p.Val782Met
XM_011518708.2:c.1132G>A XP_011517010.1:p.Val378Met
XM_017014734.1:c.2134G>A XP_016870223.1:p.Val712Met
NM_001166280.2:c.2110G>A NP_001159752.1:p.Val704Met
NM_001166281.2:c.2080G>A NP_001159753.1:p.Val694Met
NM_001369398.1:c.1108G>A NP_001356327.1:p.Val370Met
NM_005592.4:c.2368G>A MANE Select NP_005583.1:p.Val790Met