Canonical Allele Identifier: CA726646659

Gene: MYO15A

Linked Data

• dbSNP Id: rs1156246358
• MyVariant Identifiers: chr17:g.18052745del (hg19) ; chr17:g.18149431del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149434del , CM000679.2:g.18149434del	GRCh38
NC_000017.10:g.18052748del , CM000679.1:g.18052748del	GRCh37
NC_000017.9:g.17993473del	NCBI36
NG_011634.1:g.45729del
NG_011634.2:g.45729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7118-52del MANE Select	ENSP00000495481.1:n.7118-52del
ENST00000205890.9:c.7118-52del	ENSP00000205890.5:n.7118-52del
ENST00000578999.1:n.687del
ENST00000615845.4:c.7118-52del	ENSP00000481642.1:n.7118-52del
NM_016239.3:c.7118-52del	NP_057323.3:n.7118-52del
XM_011523917.1:c.6793-52del	XP_011522219.1:n.6793-52del
XM_011523921.1:c.7112-52del	XP_011522223.1:n.7112-52del
XR_934037.1:n.7452-52del
XR_934038.1:n.7404-52del
XR_934293.1:n.435-1825del
XR_934295.1:n.254-1825del
XM_017024714.2:c.7058-52del	XP_016880203.1:n.7058-52del
XM_017024715.2:c.7121-52del	XP_016880204.1:n.7121-52del
XR_934293.2:n.378-1825del
NM_016239.4:c.7118-52del MANE Select	NP_057323.3:n.7118-52del