Canonical Allele Identifier: CA2250852167
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18150374G= , CM000679.2:g.18150374G= GRCh38
NC_000017.10:g.18053688G= , CM000679.1:g.18053688G= GRCh37
NC_000017.9:g.17994413G= NCBI36
NG_011634.1:g.46669G=
NG_011634.2:g.46669G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647165.2:c.7213-55G= MANE Select ENSP00000495481.1:n.7213-55G=
ENST00000205890.9:c.7213-55G= ENSP00000205890.5:n.7213-55G=
ENST00000615845.4:c.7213-55G= ENSP00000481642.1:n.7213-55G=
NM_016239.3:c.7213-55G= NP_057323.3:n.7213-55G=
XM_011523917.1:c.6888-55G= XP_011522219.1:n.6888-55G=
XM_011523921.1:c.7207-55G= XP_011522223.1:n.7207-55G=
XR_934037.1:n.7547-55G=
XR_934038.1:n.7499-55G=
XR_934293.1:n.434+1229C=
XR_934294.1:n.435-601C=
XR_934295.1:n.253+1229C=
XM_017024714.2:c.7153-55G= XP_016880203.1:n.7153-55G=
XM_017024715.2:c.7216-55G= XP_016880204.1:n.7216-55G=
XR_934293.2:n.377+1229C=
XR_934294.2:n.378-601C=
NM_016239.4:c.7213-55G= MANE Select NP_057323.3:n.7213-55G=