Canonical Allele Identifier: CA277140
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110668985T>G , CM000671.2:g.110668985T>G GRCh38
NC_000009.11:g.113431265T>G , CM000671.1:g.113431265T>G GRCh37
NC_000009.10:g.112471086T>G NCBI36
NG_016016.1:g.5215T>G
NG_016016.2:g.5195T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.79+2T>G MANE Select ENSP00000363571.4:n.79+2T>G
ENST00000189978.10:c.79+2T>G ENSP00000189978.6:n.79+2T>G
ENST00000374440.7:c.79+2T>G ENSP00000363563.4:n.79+2T>G
ENST00000374448.8:c.79+2T>G ENSP00000363571.4:n.79+2T>G
ENST00000416899.7:c.79+2T>G ENSP00000393608.3:n.79+2T>G
NM_001166280.1:c.79+2T>G NP_001159752.1:n.79+2T>G
NM_001166281.1:c.79+2T>G NP_001159753.1:n.79+2T>G
NM_005592.3:c.79+2T>G NP_005583.1:n.79+2T>G
XM_005251994.2:c.79+2T>G XP_005252051.1:n.79+2T>G
XM_005251995.2:c.79+2T>G XP_005252052.1:n.79+2T>G
XM_005251996.2:c.79+2T>G XP_005252053.1:n.79+2T>G
XM_011518707.1:c.79+2T>G XP_011517009.1:n.79+2T>G
XM_005251994.3:c.79+2T>G XP_005252051.1:n.79+2T>G
XM_005251995.3:c.79+2T>G XP_005252052.1:n.79+2T>G
XM_005251996.3:c.79+2T>G XP_005252053.1:n.79+2T>G
XM_017014734.1:c.79+2T>G XP_016870223.1:n.79+2T>G
NM_001166280.2:c.79+2T>G NP_001159752.1:n.79+2T>G
NM_001166281.2:c.79+2T>G NP_001159753.1:n.79+2T>G
NM_005592.4:c.79+2T>G MANE Select NP_005583.1:n.79+2T>G