Canonical Allele Identifier: CA2250874691
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18159290_18159291delinsTC , CM000679.2:g.18159290_18159291delinsTC GRCh38
NC_000017.10:g.18062604_18062605delinsTC , CM000679.1:g.18062604_18062605delinsTC GRCh37
NC_000017.9:g.18003329_18003330delinsTC NCBI36
NG_011634.1:g.55585_55586delinsTC
NG_011634.2:g.55585_55586delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000642418.1:n.1510_1511delinsTC
ENST00000643693.1:n.974_975delinsTC
ENST00000644795.1:c.964_965delinsTC ENSP00000495720.1:p.Ser322=
ENST00000646782.1:n.1906_1907delinsTC
ENST00000647165.2:c.9172_9173delinsTC MANE Select ENSP00000495481.1:p.Ser3058=
ENST00000651214.1:n.1677_1678delinsTC
ENST00000205890.9:c.9172_9173delinsTC ENSP00000205890.5:p.Ser3058=
ENST00000418233.7:c.964_965delinsTC ENSP00000408800.3:p.Ser322=
ENST00000433411.7:n.109_110delinsTC
ENST00000445289.6:n.316+1390_316+1391delinsTC
ENST00000556535.5:c.34_35delinsTC ENSP00000451782.1:p.Ser12=
ENST00000557190.5:n.74_75delinsTC
ENST00000557655.5:c.34_35delinsTC ENSP00000451925.1:p.Ser12=
ENST00000578472.5:c.34_35delinsTC ENSP00000467989.1:p.Ser12=
ENST00000615845.4:c.9172_9173delinsTC ENSP00000481642.1:p.Ser3058=
NM_016239.3:c.9172_9173delinsTC NP_057323.3:p.Ser3058=
XM_011523921.1:c.9166_9167delinsTC XP_011522223.1:p.Ser3056=
XM_017024714.2:c.9112_9113delinsTC XP_016880203.1:p.Ser3038=
XM_017024715.2:c.9175_9176delinsTC XP_016880204.1:p.Ser3059=
NM_016239.4:c.9172_9173delinsTC MANE Select NP_057323.3:p.Ser3058=