Canonical Allele Identifier: CA5184009
Gene: MUSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110695477A>G , CM000671.2:g.110695477A>G GRCh38
NC_000009.11:g.113457757A>G , CM000671.1:g.113457757A>G GRCh37
NC_000009.10:g.112497578A>G NCBI36
NG_016016.1:g.31707A>G
NG_016016.2:g.31687A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005592.4:c.433A>G MANE Select NP_005583.1:p.Met145Val
ENST00000374448.9:c.433A>G MANE Select ENSP00000363571.4:p.Met145Val
NM_001166280.1:c.433A>G NP_001159752.1:p.Met145Val
NM_001166280.2:c.433A>G NP_001159752.1:p.Met145Val
NM_001166281.1:c.433A>G NP_001159753.1:p.Met145Val
NM_001166281.2:c.433A>G NP_001159753.1:p.Met145Val
NM_005592.3:c.433A>G NP_005583.1:p.Met145Val
ENST00000189978.10:c.433A>G ENSP00000189978.6:p.Met145Val
ENST00000374439.1:c.127A>G ENSP00000363562.2:p.Met43Val
ENST00000374440.7:c.433A>G ENSP00000363563.4:p.Met145Val
ENST00000374448.8:c.433A>G ENSP00000363571.4:p.Met145Val
ENST00000416899.7:c.433A>G ENSP00000393608.3:p.Met145Val
XM_005251994.2:c.433A>G XP_005252051.1:p.Met145Val
XM_005251994.3:c.433A>G XP_005252051.1:p.Met145Val
XM_005251995.2:c.433A>G XP_005252052.1:p.Met145Val
XM_005251995.3:c.433A>G XP_005252052.1:p.Met145Val
XM_005251996.2:c.433A>G XP_005252053.1:p.Met145Val
XM_005251996.3:c.433A>G XP_005252053.1:p.Met145Val
XM_011518707.1:c.433A>G XP_011517009.1:p.Met145Val
XM_017014734.1:c.433A>G XP_016870223.1:p.Met145Val