Canonical Allele Identifier: CA2636437621

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18149405-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149409dup , CM000679.2:g.18149409dup	GRCh38
NC_000017.10:g.18052723dup , CM000679.1:g.18052723dup	GRCh37
NC_000017.9:g.17993448dup	NCBI36
NG_011634.1:g.45704dup
NG_011634.2:g.45704dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7117+33dup MANE Select	ENSP00000495481.1:n.7117+33dup
ENST00000205890.9:c.7117+33dup	ENSP00000205890.5:n.7117+33dup
ENST00000578999.1:n.662dup
ENST00000615845.4:c.7117+33dup	ENSP00000481642.1:n.7117+33dup
NM_016239.3:c.7117+33dup	NP_057323.3:n.7117+33dup
XM_011523917.1:c.6792+33dup	XP_011522219.1:n.6792+33dup
XM_011523921.1:c.7111+33dup	XP_011522223.1:n.7111+33dup
XR_934037.1:n.7451+33dup
XR_934038.1:n.7404-77dup
XR_934293.1:n.435-1800dup
XR_934295.1:n.254-1800dup
XM_017024714.2:c.7057+33dup	XP_016880203.1:n.7057+33dup
XM_017024715.2:c.7120+33dup	XP_016880204.1:n.7120+33dup
XR_934293.2:n.378-1800dup
NM_016239.4:c.7117+33dup MANE Select	NP_057323.3:n.7117+33dup