Canonical Allele Identifier: CA5184019
Gene: MUSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110695545T>C , CM000671.2:g.110695545T>C GRCh38
NC_000009.11:g.113457825T>C , CM000671.1:g.113457825T>C GRCh37
NC_000009.10:g.112497646T>C NCBI36
NG_016016.1:g.31775T>C
NG_016016.2:g.31755T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005592.4:c.486+15T>C MANE Select NP_005583.1:n.486+15T>C
ENST00000374448.9:c.486+15T>C MANE Select ENSP00000363571.4:n.486+15T>C
NM_001166280.1:c.486+15T>C NP_001159752.1:n.486+15T>C
NM_001166280.2:c.486+15T>C NP_001159752.1:n.486+15T>C
NM_001166281.1:c.486+15T>C NP_001159753.1:n.486+15T>C
NM_001166281.2:c.486+15T>C NP_001159753.1:n.486+15T>C
NM_005592.3:c.486+15T>C NP_005583.1:n.486+15T>C
ENST00000189978.10:c.486+15T>C ENSP00000189978.6:n.486+15T>C
ENST00000374439.1:c.180+15T>C ENSP00000363562.2:n.180+15T>C
ENST00000374440.7:c.486+15T>C ENSP00000363563.4:n.486+15T>C
ENST00000374448.8:c.486+15T>C ENSP00000363571.4:n.486+15T>C
ENST00000416899.7:c.486+15T>C ENSP00000393608.3:n.486+15T>C
XM_005251994.2:c.486+15T>C XP_005252051.1:n.486+15T>C
XM_005251994.3:c.486+15T>C XP_005252051.1:n.486+15T>C
XM_005251995.2:c.486+15T>C XP_005252052.1:n.486+15T>C
XM_005251995.3:c.486+15T>C XP_005252052.1:n.486+15T>C
XM_005251996.2:c.486+15T>C XP_005252053.1:n.486+15T>C
XM_005251996.3:c.486+15T>C XP_005252053.1:n.486+15T>C
XM_011518707.1:c.486+15T>C XP_011517009.1:n.486+15T>C
XM_017014734.1:c.486+15T>C XP_016870223.1:n.486+15T>C