Canonical Allele Identifier: CA2636447850

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18145917-AACATCTTCGGGAACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145923_18145937del , CM000679.2:g.18145923_18145937del	GRCh38
NC_000017.10:g.18049237_18049251del , CM000679.1:g.18049237_18049251del	GRCh37
NC_000017.9:g.17989962_17989976del	NCBI36
NG_011634.1:g.42218_42232del
NG_011634.2:g.42218_42232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6325_6339del MANE Select	ENSP00000495481.1:p.Phe2109_Ile2113del
ENST00000205890.9:c.6325_6339del	ENSP00000205890.5:p.Phe2109_Ile2113del
ENST00000615845.4:c.6325_6339del	ENSP00000481642.1:p.Phe2109_Ile2113del
NM_016239.3:c.6325_6339del	NP_057323.3:p.Phe2109_Ile2113del
XM_011523917.1:c.6265_6279del	XP_011522219.1:p.Phe2089_Ile2093del
XM_011523918.1:c.6265_6279del	XP_011522220.1:p.Phe2089_Ile2093del
XM_011523921.1:c.6319_6333del	XP_011522223.1:p.Phe2107_Ile2111del
XR_934037.1:n.6924_6938del
XR_934038.1:n.6924_6938del
XM_011523918.2:c.6265_6279del	XP_011522220.1:p.Phe2089_Ile2093del
XM_017024714.2:c.6265_6279del	XP_016880203.1:p.Phe2089_Ile2093del
XM_017024715.2:c.6328_6342del	XP_016880204.1:p.Phe2110_Ile2114del
XM_024450781.1:c.6213+1331_6213+1345del	XP_024306549.1:n.6213+1331_6213+1345del
NM_016239.4:c.6325_6339del MANE Select	NP_057323.3:p.Phe2109_Ile2113del