Canonical Allele Identifier: CA2250852166

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150372A= , CM000679.2:g.18150372A=	GRCh38
NC_000017.10:g.18053686A= , CM000679.1:g.18053686A=	GRCh37
NC_000017.9:g.17994411A=	NCBI36
NG_011634.1:g.46667A=
NG_011634.2:g.46667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7213-57A= MANE Select	ENSP00000495481.1:n.7213-57A=
ENST00000205890.9:c.7213-57A=	ENSP00000205890.5:n.7213-57A=
ENST00000615845.4:c.7213-57A=	ENSP00000481642.1:n.7213-57A=
NM_016239.3:c.7213-57A=	NP_057323.3:n.7213-57A=
XM_011523917.1:c.6888-57A=	XP_011522219.1:n.6888-57A=
XM_011523921.1:c.7207-57A=	XP_011522223.1:n.7207-57A=
XR_934037.1:n.7547-57A=
XR_934038.1:n.7499-57A=
XR_934293.1:n.434+1231T=
XR_934294.1:n.435-599T=
XR_934295.1:n.253+1231T=
XM_017024714.2:c.7153-57A=	XP_016880203.1:n.7153-57A=
XM_017024715.2:c.7216-57A=	XP_016880204.1:n.7216-57A=
XR_934293.2:n.377+1231T=
XR_934294.2:n.378-599T=
NM_016239.4:c.7213-57A= MANE Select	NP_057323.3:n.7213-57A=