Canonical Allele Identifier: CA2250785564
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18127068C= , CM000679.2:g.18127068C= GRCh38
NC_000017.10:g.18030382C= , CM000679.1:g.18030382C= GRCh37
NC_000017.9:g.17971107C= NCBI36
NG_011634.1:g.23363C=
NG_011634.2:g.23363C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647165.2:c.3942-7C= MANE Select ENSP00000495481.1:n.3942-7C=
ENST00000205890.9:c.3942-7C= ENSP00000205890.5:n.3942-7C=
ENST00000615845.4:c.3942-7C= ENSP00000481642.1:n.3942-7C=
NM_016239.3:c.3942-7C= NP_057323.3:n.3942-7C=
XM_011523917.1:c.3942-7C= XP_011522219.1:n.3942-7C=
XM_011523918.1:c.3942-7C= XP_011522220.1:n.3942-7C=
XM_011523919.1:c.3942-7C= XP_011522221.1:n.3942-7C=
XM_011523920.1:c.3942-7C= XP_011522222.1:n.3942-7C=
XM_011523921.1:c.3942-7C= XP_011522223.1:n.3942-7C=
XR_934037.1:n.4601-7C=
XR_934038.1:n.4601-7C=
XR_934039.1:n.4601-7C=
XM_011523918.2:c.3942-7C= XP_011522220.1:n.3942-7C=
XM_017024714.2:c.3942-7C= XP_016880203.1:n.3942-7C=
XM_017024715.2:c.3942-7C= XP_016880204.1:n.3942-7C=
XM_024450780.1:c.3942-7C= XP_024306548.1:n.3942-7C=
XM_024450781.1:c.3942-7C= XP_024306549.1:n.3942-7C=
XM_024450782.1:c.3942-7C= XP_024306550.1:n.3942-7C=
XR_934039.2:n.4640-7C=
NM_016239.4:c.3942-7C= MANE Select NP_057323.3:n.3942-7C=