Canonical Allele Identifier: CA5184471
Gene: MUSK HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110787683C>T , CM000671.2:g.110787683C>T GRCh38
NC_000009.11:g.113549963C>T , CM000671.1:g.113549963C>T GRCh37
NC_000009.10:g.112589784C>T NCBI36
NG_016016.1:g.123913C>T
NG_016016.2:g.123893C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.1779-7C>T MANE Select ENSP00000363571.4:n.1779-7C>T
ENST00000189978.10:c.1521-7C>T ENSP00000189978.6:n.1521-7C>T
ENST00000374438.1:n.810-7C>T
ENST00000374440.7:c.1521-7C>T ENSP00000363563.4:n.1521-7C>T
ENST00000374448.8:c.1779-7C>T ENSP00000363571.4:n.1779-7C>T
ENST00000416899.7:c.1755-7C>T ENSP00000393608.3:n.1755-7C>T
NM_001166280.1:c.1521-7C>T NP_001159752.1:n.1521-7C>T
NM_001166281.1:c.1491-7C>T NP_001159753.1:n.1491-7C>T
NM_005592.3:c.1779-7C>T NP_005583.1:n.1779-7C>T
XM_005251994.2:c.1809-7C>T XP_005252051.1:n.1809-7C>T
XM_005251995.2:c.1785-7C>T XP_005252052.1:n.1785-7C>T
XM_005251996.2:c.1755-7C>T XP_005252053.1:n.1755-7C>T
XM_011518707.1:c.1839-7C>T XP_011517009.1:n.1839-7C>T
XM_011518708.1:c.543-7C>T XP_011517010.1:n.543-7C>T
XM_005251994.3:c.1809-7C>T XP_005252051.1:n.1809-7C>T
XM_005251995.3:c.1785-7C>T XP_005252052.1:n.1785-7C>T
XM_005251996.3:c.1755-7C>T XP_005252053.1:n.1755-7C>T
XM_011518708.2:c.543-7C>T XP_011517010.1:n.543-7C>T
XM_017014734.1:c.1545-7C>T XP_016870223.1:n.1545-7C>T
NM_001166280.2:c.1521-7C>T NP_001159752.1:n.1521-7C>T
NM_001166281.2:c.1491-7C>T NP_001159753.1:n.1491-7C>T
NM_001369398.1:c.519-7C>T NP_001356327.1:n.519-7C>T
NM_005592.4:c.1779-7C>T MANE Select NP_005583.1:n.1779-7C>T