Canonical Allele Identifier: CA8472114

Gene: MYO18A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29092886C>T , CM000679.2:g.29092886C>T	GRCh38
NC_000017.10:g.27419904C>T , CM000679.1:g.27419904C>T	GRCh37
NC_000017.9:g.24444030C>T	NCBI36
NG_051989.1:g.92504G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704659.1:c.5078G>A	ENSP00000515984.1:p.Ser1693Asn
ENST00000527372.7:c.5042G>A MANE Select	ENSP00000437073.1:p.Ser1681Asn
ENST00000527372.5:c.5042G>A	ENSP00000437073.1:p.Ser1681Asn
ENST00000530254.6:c.4152G>A
ENST00000531253.5:c.5042G>A	ENSP00000434228.1:p.Ser1681Asn
ENST00000533112.5:c.4931G>A	ENSP00000435932.1:p.Ser1644Asn
ENST00000628822.2:c.5039G>A	ENSP00000486682.1:p.Ser1680Asn
NM_078471.3:c.5042G>A	NP_510880.2:p.Ser1681Asn
NM_203318.1:c.5042G>A	NP_976063.1:p.Ser1681Asn
NM_001346765.1:c.5099G>A	NP_001333694.1:p.Ser1700Asn
NM_001346766.1:c.5078G>A	NP_001333695.1:p.Ser1693Asn
NM_001346767.1:c.4931G>A	NP_001333696.1:p.Ser1644Asn
NM_001346768.1:c.3668G>A	NP_001333697.1:p.Ser1223Asn
NM_001346765.2:c.5099G>A	NP_001333694.1:p.Ser1700Asn
NM_001346766.2:c.5078G>A	NP_001333695.1:p.Ser1693Asn
NM_001346767.2:c.4931G>A	NP_001333696.1:p.Ser1644Asn
NM_001346768.2:c.3668G>A	NP_001333697.1:p.Ser1223Asn
NM_078471.4:c.5042G>A MANE Select	NP_510880.2:p.Ser1681Asn
NM_203318.2:c.5042G>A	NP_976063.1:p.Ser1681Asn