Canonical Allele Identifier: CA8471982

Gene: MYO18A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29090089G>C , CM000679.2:g.29090089G>C	GRCh38
NC_000017.10:g.27417107G>C , CM000679.1:g.27417107G>C	GRCh37
NC_000017.9:g.24441233G>C	NCBI36
NG_051989.1:g.95301C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_078471.4:c.5398C>G MANE Select	NP_510880.2:p.Leu1800Val
ENST00000527372.7:c.5398C>G MANE Select	ENSP00000437073.1:p.Leu1800Val
NM_001346765.1:c.5455C>G	NP_001333694.1:p.Leu1819Val
NM_001346765.2:c.5455C>G	NP_001333694.1:p.Leu1819Val
NM_001346766.1:c.5434C>G	NP_001333695.1:p.Leu1812Val
NM_001346766.2:c.5434C>G	NP_001333695.1:p.Leu1812Val
NM_001346767.1:c.5287C>G	NP_001333696.1:p.Leu1763Val
NM_001346767.2:c.5287C>G	NP_001333696.1:p.Leu1763Val
NM_001346768.1:c.4024C>G	NP_001333697.1:p.Leu1342Val
NM_001346768.2:c.4024C>G	NP_001333697.1:p.Leu1342Val
NM_078471.3:c.5398C>G	NP_510880.2:p.Leu1800Val
NM_203318.1:c.5398C>G	NP_976063.1:p.Leu1800Val
NM_203318.2:c.5398C>G	NP_976063.1:p.Leu1800Val
ENST00000527372.5:c.5398C>G	ENSP00000437073.1:p.Leu1800Val
ENST00000529578.5:n.692C>G
ENST00000529889.1:n.378C>G
ENST00000530254.6:c.4508C>G
ENST00000531253.5:c.5398C>G	ENSP00000434228.1:p.Leu1800Val
ENST00000531438.5:n.72C>G
ENST00000531892.5:n.120C>G
ENST00000533112.5:c.5287C>G	ENSP00000435932.1:p.Leu1763Val
ENST00000546105.5:n.431C>G
ENST00000628822.2:c.5395C>G	ENSP00000486682.1:p.Leu1799Val
ENST00000704659.1:c.5434C>G	ENSP00000515984.1:p.Leu1812Val