Canonical Allele Identifier: CA5183939
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110682810C>T , CM000671.2:g.110682810C>T GRCh38
NC_000009.11:g.113445090C>T , CM000671.1:g.113445090C>T GRCh37
NC_000009.10:g.112484911C>T NCBI36
NG_016016.1:g.19040C>T
NG_016016.2:g.19020C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.206+10C>T MANE Select ENSP00000363571.4:n.206+10C>T
ENST00000189978.10:c.206+10C>T ENSP00000189978.6:n.206+10C>T
ENST00000374440.7:c.206+10C>T ENSP00000363563.4:n.206+10C>T
ENST00000374448.8:c.206+10C>T ENSP00000363571.4:n.206+10C>T
ENST00000416899.7:c.206+10C>T ENSP00000393608.3:n.206+10C>T
NM_001166280.1:c.206+10C>T NP_001159752.1:n.206+10C>T
NM_001166281.1:c.206+10C>T NP_001159753.1:n.206+10C>T
NM_005592.3:c.206+10C>T NP_005583.1:n.206+10C>T
XM_005251994.2:c.206+10C>T XP_005252051.1:n.206+10C>T
XM_005251995.2:c.206+10C>T XP_005252052.1:n.206+10C>T
XM_005251996.2:c.206+10C>T XP_005252053.1:n.206+10C>T
XM_011518707.1:c.206+10C>T XP_011517009.1:n.206+10C>T
XM_005251994.3:c.206+10C>T XP_005252051.1:n.206+10C>T
XM_005251995.3:c.206+10C>T XP_005252052.1:n.206+10C>T
XM_005251996.3:c.206+10C>T XP_005252053.1:n.206+10C>T
XM_017014734.1:c.206+10C>T XP_016870223.1:n.206+10C>T
NM_001166280.2:c.206+10C>T NP_001159752.1:n.206+10C>T
NM_001166281.2:c.206+10C>T NP_001159753.1:n.206+10C>T
NM_005592.4:c.206+10C>T MANE Select NP_005583.1:n.206+10C>T