Canonical Allele Identifier: CA2250853896
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18151952G= , CM000679.2:g.18151952G= GRCh38
NC_000017.10:g.18055266G= , CM000679.1:g.18055266G= GRCh37
NC_000017.9:g.17995991G= NCBI36
NG_011634.1:g.48247G=
NG_011634.2:g.48247G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7893+1G= MANE Select ENSP00000495481.1:n.7893+1G=
ENST00000205890.9:c.7893+1G= ENSP00000205890.5:n.7893+1G=
ENST00000615845.4:c.7893+1G= ENSP00000481642.1:n.7893+1G=
NM_016239.3:c.7893+1G= NP_057323.3:n.7893+1G=
XM_011523921.1:c.7887+1G= XP_011522223.1:n.7887+1G=
XR_934293.1:n.131-46C=
XR_934294.1:n.131-46C=
XR_934295.1:n.131-227C=
XM_017024714.2:c.7833+1G= XP_016880203.1:n.7833+1G=
XM_017024715.2:c.7896+1G= XP_016880204.1:n.7896+1G=
XR_934293.2:n.74-46C=
XR_934294.2:n.74-46C=
NM_016239.4:c.7893+1G= MANE Select NP_057323.3:n.7893+1G=