Canonical Allele Identifier: CA2250852200
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18150445C= , CM000679.2:g.18150445C= GRCh38
NC_000017.10:g.18053759C= , CM000679.1:g.18053759C= GRCh37
NC_000017.9:g.17994484C= NCBI36
NG_011634.1:g.46740C=
NG_011634.2:g.46740C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7229C= MANE Select ENSP00000495481.1:p.Thr2410=
ENST00000205890.9:c.7229C= ENSP00000205890.5:p.Thr2410=
ENST00000615845.4:c.7229C= ENSP00000481642.1:p.Thr2410=
NM_016239.3:c.7229C= NP_057323.3:p.Thr2410=
XM_011523917.1:c.6904C= XP_011522219.1:p.Gln2302=
XM_011523921.1:c.7223C= XP_011522223.1:p.Thr2408=
XR_934037.1:n.7563C=
XR_934038.1:n.7515C=
XR_934293.1:n.434+1158G=
XR_934294.1:n.435-672G=
XR_934295.1:n.253+1158G=
XM_017024714.2:c.7169C= XP_016880203.1:p.Thr2390=
XM_017024715.2:c.7232C= XP_016880204.1:p.Thr2411=
XR_934293.2:n.377+1158G=
XR_934294.2:n.378-672G=
NM_016239.4:c.7229C= MANE Select NP_057323.3:p.Thr2410=