Canonical Allele Identifier: CA374665273
Gene: MUSK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.110695530G>T , CM000671.2:g.110695530G>T GRCh38
NC_000009.11:g.113457810G>T , CM000671.1:g.113457810G>T GRCh37
NC_000009.10:g.112497631G>T NCBI36
NG_016016.1:g.31760G>T
NG_016016.2:g.31740G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374448.9:c.486G>T MANE Select ENSP00000363571.4:p.Arg162Ser
ENST00000189978.10:c.486G>T ENSP00000189978.6:p.Arg162Ser
ENST00000374439.1:c.180G>T ENSP00000363562.2:p.Arg60Ser
ENST00000374440.7:c.486G>T ENSP00000363563.4:p.Arg162Ser
ENST00000374448.8:c.486G>T ENSP00000363571.4:p.Arg162Ser
ENST00000416899.7:c.486G>T ENSP00000393608.3:p.Arg162Ser
NM_001166280.1:c.486G>T NP_001159752.1:p.Arg162Ser
NM_001166281.1:c.486G>T NP_001159753.1:p.Arg162Ser
NM_005592.3:c.486G>T NP_005583.1:p.Arg162Ser
XM_005251994.2:c.486G>T XP_005252051.1:p.Arg162Ser
XM_005251995.2:c.486G>T XP_005252052.1:p.Arg162Ser
XM_005251996.2:c.486G>T XP_005252053.1:p.Arg162Ser
XM_011518707.1:c.486G>T XP_011517009.1:p.Arg162Ser
XM_005251994.3:c.486G>T XP_005252051.1:p.Arg162Ser
XM_005251995.3:c.486G>T XP_005252052.1:p.Arg162Ser
XM_005251996.3:c.486G>T XP_005252053.1:p.Arg162Ser
XM_017014734.1:c.486G>T XP_016870223.1:p.Arg162Ser
NM_001166280.2:c.486G>T NP_001159752.1:p.Arg162Ser
NM_001166281.2:c.486G>T NP_001159753.1:p.Arg162Ser
NM_005592.4:c.486G>T MANE Select NP_005583.1:p.Arg162Ser