Canonical Allele Identifier: CA398450016

Gene: MYO18A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29074058A>C , CM000679.2:g.29074058A>C	GRCh38
NC_000017.10:g.27401076A>C , CM000679.1:g.27401076A>C	GRCh37
NC_000017.9:g.24425202A>C	NCBI36
NG_051989.1:g.111332T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704659.1:c.*712T>G	ENSP00000515984.1:n.*712T>G
ENST00000527372.7:c.*712T>G MANE Select	ENSP00000437073.1:n.*712T>G
ENST00000359450.6:c.142T>G	ENSP00000352424.6:p.Tyr48Asp
ENST00000527372.5:c.*712T>G	ENSP00000437073.1:n.*712T>G
ENST00000529578.5:n.2126T>G
ENST00000530254.6:c.5942T>G
ENST00000531253.5:c.*712T>G	ENSP00000434228.1:n.*712T>G
ENST00000533112.5:c.*712T>G	ENSP00000435932.1:n.*712T>G
ENST00000628822.2:c.*712T>G	ENSP00000486682.1:n.*712T>G
NM_004740.3:c.142T>G	NP_004731.2:p.Tyr48Asp
NM_078471.3:c.*712T>G	NP_510880.2:n.*712T>G
NM_203318.1:c.*712T>G	NP_976063.1:n.*712T>G
NM_001346765.1:c.*712T>G	NP_001333694.1:n.*712T>G
NM_001346766.1:c.*712T>G	NP_001333695.1:n.*712T>G
NM_001346767.1:c.*712T>G	NP_001333696.1:n.*712T>G
NM_001346768.1:c.*712T>G	NP_001333697.1:n.*712T>G
NM_001346765.2:c.*712T>G	NP_001333694.1:n.*712T>G
NM_001346766.2:c.*712T>G	NP_001333695.1:n.*712T>G
NM_001346767.2:c.*712T>G	NP_001333696.1:n.*712T>G
NM_001346768.2:c.*712T>G	NP_001333697.1:n.*712T>G
NM_078471.4:c.*712T>G MANE Select	NP_510880.2:n.*712T>G
NM_203318.2:c.*712T>G	NP_976063.1:n.*712T>G