Canonical Allele Identifier: CA8472429

Gene: MYO18A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29097839G>A , CM000679.2:g.29097839G>A	GRCh38
NC_000017.10:g.27424857G>A , CM000679.1:g.27424857G>A	GRCh37
NC_000017.9:g.24448983G>A	NCBI36
NG_051989.1:g.87551C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_078471.4:c.4051C>T MANE Select	NP_510880.2:p.Arg1351Cys
ENST00000527372.7:c.4051C>T MANE Select	ENSP00000437073.1:p.Arg1351Cys
NM_001346765.1:c.4108C>T	NP_001333694.1:p.Arg1370Cys
NM_001346765.2:c.4108C>T	NP_001333694.1:p.Arg1370Cys
NM_001346766.1:c.4087C>T	NP_001333695.1:p.Arg1363Cys
NM_001346766.2:c.4087C>T	NP_001333695.1:p.Arg1363Cys
NM_001346767.1:c.4051C>T	NP_001333696.1:p.Arg1351Cys
NM_001346767.2:c.4051C>T	NP_001333696.1:p.Arg1351Cys
NM_001346768.1:c.2677C>T	NP_001333697.1:p.Arg893Cys
NM_001346768.2:c.2677C>T	NP_001333697.1:p.Arg893Cys
NM_078471.3:c.4051C>T	NP_510880.2:p.Arg1351Cys
NM_203318.1:c.4051C>T	NP_976063.1:p.Arg1351Cys
NM_203318.2:c.4051C>T	NP_976063.1:p.Arg1351Cys
ENST00000527372.5:c.4051C>T	ENSP00000437073.1:p.Arg1351Cys
ENST00000530254.6:c.3161C>T
ENST00000530557.2:n.42C>T
ENST00000531253.5:c.4051C>T	ENSP00000434228.1:p.Arg1351Cys
ENST00000533112.5:c.4051C>T	ENSP00000435932.1:p.Arg1351Cys
ENST00000628822.2:c.4048C>T	ENSP00000486682.1:p.Arg1350Cys
ENST00000704659.1:c.4087C>T	ENSP00000515984.1:p.Arg1363Cys