Canonical Allele Identifier: CA273603

Gene: MYO15A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18171691C>A , CM000679.2:g.18171691C>A	GRCh38
NC_000017.10:g.18075005C>A , CM000679.1:g.18075005C>A	GRCh37
NC_000017.9:g.18015730C>A	NCBI36
NG_011634.1:g.67986C>A
NG_011634.2:g.67986C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.2540C>A
ENST00000643693.1:n.2078C>A
ENST00000644795.1:c.1928C>A	ENSP00000495720.1:p.Ser643Ter
ENST00000646782.1:n.2870C>A
ENST00000647165.2:c.10136C>A MANE Select	ENSP00000495481.1:p.Ser3379Ter
ENST00000651214.1:n.2567C>A
ENST00000205890.9:c.10136C>A	ENSP00000205890.5:p.Ser3379Ter
ENST00000418233.7:c.1928C>A	ENSP00000408800.3:p.Ser643Ter
ENST00000433411.7:n.1586C>A
ENST00000445289.6:n.905C>A
ENST00000578575.1:c.678C>A
ENST00000579848.6:c.556C>A	ENSP00000465910.1:p.Arg186=
ENST00000615845.4:c.10136C>A	ENSP00000481642.1:p.Ser3379Ter
NM_016239.3:c.10136C>A	NP_057323.3:p.Ser3379Ter
XM_011523921.1:c.10130C>A	XP_011522223.1:p.Ser3377Ter
XM_017024714.2:c.10076C>A	XP_016880203.1:p.Ser3359Ter
XM_017024715.2:c.10139C>A	XP_016880204.1:p.Ser3380Ter
NM_016239.4:c.10136C>A MANE Select	NP_057323.3:p.Ser3379Ter