Canonical Allele Identifier: CA5184311
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110775853C>T , CM000671.2:g.110775853C>T GRCh38
NC_000009.11:g.113538133C>T , CM000671.1:g.113538133C>T GRCh37
NC_000009.10:g.112577954C>T NCBI36
NG_016016.1:g.112083C>T
NG_016016.2:g.112063C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.1250C>T MANE Select ENSP00000363571.4:p.Thr417Ile
ENST00000189978.10:c.1016C>T ENSP00000189978.6:p.Thr339Ile
ENST00000374438.1:n.507C>T
ENST00000374440.7:c.1016C>T ENSP00000363563.4:p.Thr339Ile
ENST00000374448.8:c.1250C>T ENSP00000363571.4:p.Thr417Ile
ENST00000416899.7:c.1250C>T ENSP00000393608.3:p.Thr417Ile
NM_001166280.1:c.1016C>T NP_001159752.1:p.Thr339Ile
NM_001166281.1:c.986C>T NP_001159753.1:p.Thr329Ile
NM_005592.3:c.1250C>T NP_005583.1:p.Thr417Ile
XM_005251994.2:c.1280C>T XP_005252051.1:p.Thr427Ile
XM_005251995.2:c.1280C>T XP_005252052.1:p.Thr427Ile
XM_005251996.2:c.1250C>T XP_005252053.1:p.Thr417Ile
XM_011518707.1:c.1310C>T XP_011517009.1:p.Thr437Ile
XM_011518708.1:c.14C>T XP_011517010.1:p.Thr5Ile
XM_005251994.3:c.1280C>T XP_005252051.1:p.Thr427Ile
XM_005251995.3:c.1280C>T XP_005252052.1:p.Thr427Ile
XM_005251996.3:c.1250C>T XP_005252053.1:p.Thr417Ile
XM_011518708.2:c.14C>T XP_011517010.1:p.Thr5Ile
XM_017014734.1:c.1016C>T XP_016870223.1:p.Thr339Ile
XR_001746892.1:n.288+8960G>A
NM_001166280.2:c.1016C>T NP_001159752.1:p.Thr339Ile
NM_001166281.2:c.986C>T NP_001159753.1:p.Thr329Ile
NM_001369398.1:c.14C>T NP_001356327.1:p.Thr5Ile
NM_005592.4:c.1250C>T MANE Select NP_005583.1:p.Thr417Ile