Canonical Allele Identifier: CA2250851752

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149428T= , CM000679.2:g.18149428T=	GRCh38
NC_000017.10:g.18052742T= , CM000679.1:g.18052742T=	GRCh37
NC_000017.9:g.17993467T=	NCBI36
NG_011634.1:g.45723T=
NG_011634.2:g.45723T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7117+52T= MANE Select	ENSP00000495481.1:n.7117+52T=
ENST00000205890.9:c.7117+52T=	ENSP00000205890.5:n.7117+52T=
ENST00000578999.1:n.681T=
ENST00000615845.4:c.7117+52T=	ENSP00000481642.1:n.7117+52T=
NM_016239.3:c.7117+52T=	NP_057323.3:n.7117+52T=
XM_011523917.1:c.6792+52T=	XP_011522219.1:n.6792+52T=
XM_011523921.1:c.7111+52T=	XP_011522223.1:n.7111+52T=
XR_934037.1:n.7451+52T=
XR_934038.1:n.7404-58T=
XR_934293.1:n.435-1822A=
XR_934295.1:n.254-1822A=
XM_017024714.2:c.7057+52T=	XP_016880203.1:n.7057+52T=
XM_017024715.2:c.7120+52T=	XP_016880204.1:n.7120+52T=
XR_934293.2:n.378-1822A=
NM_016239.4:c.7117+52T= MANE Select	NP_057323.3:n.7117+52T=