Canonical Allele Identifier: CA5184434
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110785664T>C , CM000671.2:g.110785664T>C GRCh38
NC_000009.11:g.113547944T>C , CM000671.1:g.113547944T>C GRCh37
NC_000009.10:g.112587765T>C NCBI36
NG_016016.1:g.121894T>C
NG_016016.2:g.121874T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.1724T>C MANE Select ENSP00000363571.4:p.Ile575Thr
ENST00000189978.10:c.1466T>C ENSP00000189978.6:p.Ile489Thr
ENST00000374438.1:n.755T>C
ENST00000374440.7:c.1466T>C ENSP00000363563.4:p.Ile489Thr
ENST00000374448.8:c.1724T>C ENSP00000363571.4:p.Ile575Thr
ENST00000416899.7:c.1700T>C ENSP00000393608.3:p.Ile567Thr
NM_001166280.1:c.1466T>C NP_001159752.1:p.Ile489Thr
NM_001166281.1:c.1436T>C NP_001159753.1:p.Ile479Thr
NM_005592.3:c.1724T>C NP_005583.1:p.Ile575Thr
XM_005251994.2:c.1754T>C XP_005252051.1:p.Ile585Thr
XM_005251995.2:c.1730T>C XP_005252052.1:p.Ile577Thr
XM_005251996.2:c.1700T>C XP_005252053.1:p.Ile567Thr
XM_011518707.1:c.1784T>C XP_011517009.1:p.Ile595Thr
XM_011518708.1:c.488T>C XP_011517010.1:p.Ile163Thr
XM_005251994.3:c.1754T>C XP_005252051.1:p.Ile585Thr
XM_005251995.3:c.1730T>C XP_005252052.1:p.Ile577Thr
XM_005251996.3:c.1700T>C XP_005252053.1:p.Ile567Thr
XM_011518708.2:c.488T>C XP_011517010.1:p.Ile163Thr
XM_017014734.1:c.1490T>C XP_016870223.1:p.Ile497Thr
XR_001746892.1:n.59A>G
NM_001166280.2:c.1466T>C NP_001159752.1:p.Ile489Thr
NM_001166281.2:c.1436T>C NP_001159753.1:p.Ile479Thr
NM_001369398.1:c.464T>C NP_001356327.1:p.Ile155Thr
NM_005592.4:c.1724T>C MANE Select NP_005583.1:p.Ile575Thr