Canonical Allele Identifier: CA398588981

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18027800C>G (hg19) ; chr17:g.18124486C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18124486C>G , CM000679.2:g.18124486C>G	GRCh38
NC_000017.10:g.18027800C>G , CM000679.1:g.18027800C>G	GRCh37
NC_000017.9:g.17968525C>G	NCBI36
NG_011634.1:g.20781C>G
NG_011634.2:g.20781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.3613C>G MANE Select	ENSP00000495481.1:p.His1205Asp
ENST00000651088.1:c.154C>G	ENSP00000498988.1:p.His52Asp
ENST00000205890.9:c.3613C>G	ENSP00000205890.5:p.His1205Asp
ENST00000583079.1:n.5319C>G
ENST00000615845.4:c.3613C>G	ENSP00000481642.1:p.His1205Asp
NM_016239.3:c.3613C>G	NP_057323.3:p.His1205Asp
XM_011523917.1:c.3613C>G	XP_011522219.1:p.His1205Asp
XM_011523918.1:c.3613C>G	XP_011522220.1:p.His1205Asp
XM_011523919.1:c.3613C>G	XP_011522221.1:p.His1205Asp
XM_011523920.1:c.3613C>G	XP_011522222.1:p.His1205Asp
XM_011523921.1:c.3613C>G	XP_011522223.1:p.His1205Asp
XR_934037.1:n.4272C>G
XR_934038.1:n.4272C>G
XR_934039.1:n.4272C>G
XM_011523918.2:c.3613C>G	XP_011522220.1:p.His1205Asp
XM_017024714.2:c.3613C>G	XP_016880203.1:p.His1205Asp
XM_017024715.2:c.3613C>G	XP_016880204.1:p.His1205Asp
XM_024450780.1:c.3613C>G	XP_024306548.1:p.His1205Asp
XM_024450781.1:c.3613C>G	XP_024306549.1:p.His1205Asp
XM_024450782.1:c.3613C>G	XP_024306550.1:p.His1205Asp
XR_934039.2:n.4311C>G
NM_016239.4:c.3613C>G MANE Select	NP_057323.3:p.His1205Asp